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[1, 1?-Bis (di-cyclohexylphosphino) ferrocene]dichloropalladium (II) Quick inquiry Where to buy Suppliers range | red crystalline powder. Uses: 1,1'-Bis(di-cyclohexylphosphino)ferrocene palladium dichloride is an air-stable catalyst useful in the arylation of various ketones with aryl chlorides and aryl bromides. Group: Palladium series catalysts. Alternative Names: PdCl2(dcypf). Grades: Pd >14.0%. CAS No. 917511-90-1. Molecular formula: C34H52Cl2FeP2Pd. Mole weight: 755.90. IUPAC Name: dichloropalladium; dicyclohexyl(cyclopentyl)phosphane; iron. Exact Mass: 754.13100. Melting Point: 294-300ºC. SMILES: C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. Cl[Pd]Cl. [Fe]. InChIKey: HRAMBTUEZQOQRK-UHFFFAOYSA-L. | |
1,1?-Bis(di-isopropylphosphino)ferrocene palladium dichloride Quick inquiry Where to buy Suppliers range | red crystalline powder. Uses: Palladium-catalyzed P-C bond formation between diphenylphosphine and ortho-substituted aryl bromides. Deoxygenation of pyridine N-oxides by palladium-catalyzed oxidation of trialkylamines Air-stable catalyst useful in challenging Suzuki coupling reactions. Group: Palladium series catalysts. Alternative Names: PdCl2(dippf). Grades: Pd >17.5%. CAS No. 215788-65-1. Molecular formula: C22H36Cl2FeP2Pd. Mole weight: 595.64. IUPAC Name: cyclopentyl-di(propan-2-yl)phosphane;dichloropalladium;iron. Exact Mass: 594.00500. Melting Point: 282-287 °C. SMILES: CC(C)P([C]1[CH][CH][CH][CH]1)C(C)C. CC(C)P([C]1[CH][CH][CH][CH]1)C(C)C. Cl[Pd]Cl. [Fe]. InChIKey: UXOSTJATWDHIKQ-UHFFFAOYSA-L. | |
[1'1-bis (diphenylphosphino) ferrocene]dichloropalladium dichloromethane complex, Pd : 13.0 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: [1'1-bis (diphenylphosphino) ferrocene]dichloropalladium dichloromethane complex is used as the research compound. Group: Colloidal Catalysts. CAS No. 95564-05-4. Molecular Weight: 816.64 g/mol. | |
[1, 1?-Bis (diphenylphosphino) ferrocene] dichloropalladium (II) Quick inquiry Where to buy Suppliers range | [1, 1?-Bis (diphenylphosphino) ferrocene] dichloropalladium (II) , is a palladium catalyst used in chemical synthesis of various compounds. Group: Biochemicals. Grades: Highly Purified. CAS No. 72287-26-4. Pack Sizes: 500mg, 1g. Molecular Formula: C34H28FeP2 ·PdCl2. US Biological Life Sciences. | Worldwide |
1,1-bis(diphenylphosphino)ferrocene palladium dichloride, Pd : 14.5 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·For carbonylation reaction, cross-coupling reaction, Suzuki reaction catalyst. Group: Colloidal Catalysts. CAS No. 72287-26-4. Molecular Weight: 731.7 g/mol. SMILES: [Fe]. Cl[Pd]Cl. [CH]1[CH][CH][C] ([CH]1)P (c2ccccc2)c3ccccc3. [CH]4[CH][CH][C] ([CH]4)P (c5ccccc5)c6ccccc6. InChI: JCWIWBWXCVGEAN-UHFFFAOYSA-L. Boiling Point: 266-283 °C (lit.). Density: Soluble in dichloromethane. | |
[1, 1'-Bis (diphenylphosphino) ferrocene]palladium (II) Dichloride Dichloromethane Adduct Quick inquiry Where to buy Suppliers range | orange-red crystals. Uses: Catalyst for the borylation of aryl halides. β-Alkyl Suzuki-Miyaura cross-coupling reactions with potassium alkyltrifluoroborates. Catalyst for modified Negishi coupling. Synthesis of polyheterocycles by a Pd-catalyzed intramolecular N-arylation/C-H bond activation/aryl-aryl bond-forming domino process. Catalyst for Stille allylation. Catalyst for the amination of aryl bromides. Group: Other. Alternative Names: Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) Dichloromethane Adduct. Grades: Pd ≥13.0%. CAS No. 95464-05-4. Molecular formula: C34H28Cl2FeP2Pd·CH2Cl2. Mole weight: 816.64. IUPAC Name: [1, 1-Bis (diphenylphosphino) ferrocene]dichloropalladium (II) , complex wi. Exact Mass: 823.97400. Symbol: GHS07. Density: 1 g/cm3. Safty Description: Warning. Hazard statements: H302-H312-H315-H319-H332. | |
1,1'-Bis(di-tert-butylphosphino)ferrocene Quick inquiry Where to buy Suppliers range | Dark-yellow powder. Uses: Ligand for synthesis of polycyclic indoles via Pd-catalyzed intramolecular heteroannulation. Ligand for the palladium-catalyzed intramolecular arylation of aryl bromides under mild conditions. Ligand for cross-coupling reactions between bromoarenes and potassium allyltrifluoroborates promoted by a catalyst prepared from Pd(OAc)2 and DTBPF selectively providing γ-coupling products. Ligand for the copper-catalyzed system for the ß-boration of of a variety of α,ß-unsaturated amides. Ligand for the synthesis of Paucifloral F and related indanone analogues via palladium-catalyzed α-arylation. Ligand for the Pd-carbon monoxide complex catalyzed hydroxycarbonylation of aryl halides. Ligand for the palladium-catalyzed β-C-glycosylation by decarboxylative allylation to normal pyran systems,and cis-2,6-disubstituted tetrahydropyrans. Pd-catalyzed dearomative indole bisfunctionalization via a diastereoselective arylcyanation. Ligand for the copper- DTBPF catalyzed C-H activation and carboxylation of terminal alkynes. Group: Organic Phosphine Compounds. Alternative Names: 1,1-BIS(DI-TERT-BUTYLPHOSPHINO)FERROCENE. Grades: 98%. CAS No. 84680-95-5. Molecular formula: C26H44FeP2. Mole weight: 474.43. IUPAC Name: 1,1-Bis(di-tert-butylphosphino)ferrocene. Exact Mass: 474.22700. Melting Point: 73-75ºC. Safty Description: S26-S36/37/39. Hazard statements: Xi: Irritant. | |
[1, 1'-Bis (di-tert-butylphosphino)ferrocene]palladium (II) Dichloride Quick inquiry Where to buy Suppliers range | dark red crystals. Uses: 1,1'-Bis (di-t-butylphosphino)ferrocene palladium dichloride is used as a catalyst for the preparation of chalcones. Group: Palladium series catalysts. Alternative Names: PdCl2(dtbpf). Grades: Pd ≥16.3%. CAS No. 95408-45-0. Molecular formula: C26H44Cl2FeP2Pd. Mole weight: 651.75. IUPAC Name: Dichloro[1, 1-Bis (di-Tert-Butylphosphino)Ferrocene]Palladium (II). Exact Mass: 650.06800. Melting Point: 203-208 °C. | |
(+)-1,2-Bis((2R,5R)-2,5-di-i-propylphospholano)benzene)1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, min. 98% (R,R)-i-Pr-DUPHOS-Rh Quick inquiry Where to buy Suppliers range | (+)-1,2-Bis((2R,5R)-2,5-di-i-propylphospholano)benzene)1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, min. 98% (R,R)-i-Pr-DUPHOS-Rh. Uses: The DUPHOS family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. Efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides. Forms superior catalysts for asymmetric reductive aminations. Catalyst used for the asymmetric hydrogenation of enol phosphonates. A novel enantioselective synthesis of β-amino alcohols and 1,2-diamines. Ligand for the catalytic asymmetric [4+1] cycloaddition of vinylallenes with CO. Ligand for the Rh-catalyzed asymmetric enyne cycloisomerization. Catalytic enantioselective addition of dialkylzinc to N-Diphenylphosphinoylimines. Palladium catalyzed asymmetric phosphination. Group: Heterocyclic Organic Compound. Alternative Names: 569650-64-2;1,2-Bis[(2R,5R)-2,5-diisopropylphospholano]benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; (R, R)-i-Pr-DUPHOS-Rh; DTXSID00514132; PUBCHEM_12964416; MFCD07369039; (+)-1, 2-Bis((2R, 5R)-2, 5-di-i-propylphospholano)benzene(1, 5-cyclooctadiene)rhodium(I) tetrafluoroborate; (+)-1, 2-Bis ( (2R, 5R)-2, 5-di-i-propylphospholano)benzene)1, 5-cyclooctadiene)rhodium (i)tetrafluoroborate. CAS No. 569650-64-2. Molecular formula: C34H56BF4P2Rh-. Mole weight: 716.479g/mol. IUPAC Name: (1Z, 5Z)-cycloocta-1, 5-diene; (2R, 5R)-1-[2-[(2R, 5R)-2, 5-di(propan-2-yl)phospholan-1-yl]phenyl]-2, 5-di(propan-2-yl)phospholane; rhodium; tetrafluoroborate. Rotatable Bond Count: 6. Exact Mass: 716.294g/mol. SMILES: [B-] (F) (F) (F)F. CC (C)C1CCC (P1C2=CC=CC=C2P3C (CCC3C (C)C)C (C)C)C (C)C. C1CC=CCCC=C1. [Rh]. InChI: InChI=1S/C26H44P2.C8H12.BF4.Rh/c1-17(2)21-13-14-22(18(3)4)27(21)25-11-9-10-12-26(25)28-23(19(5)6)15-16-24(28)20(7)8;1-2-4-6-8-7-5-3-1;2-1(3,4)5;/h9-12,17-24H,13-16H2,1-8H3;1-2,7-8H,3-6H2;;/q;;-1;/b;2-1-,8-7-;;/t21-,22-,23-,24-;;;/m1./s1. InChIKey: IJKOQQHIAGRJHA-QPZXYOTCSA-N. H-Bond Acceptor: 5. Monoisotopic Mass: 716.294g/mol. | |
(-)-1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (R,R)-Me-DUPHOS-Rh Quick inquiry Where to buy Suppliers range | (-)-1,2-Bis((2R,5R)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (R,R)-Me-DUPHOS-Rh. Uses: The DUPHOS family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. Efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides. Forms superior catalysts for asymmetric reductive aminations. Catalyst used for the asymmetric hydrogenation of enol phosphonates. A novel enantioselective synthesis of β-amino alcohols and 1,2-diamines. Ligand for the catalytic asymmetric [4+1] cycloaddition of vinylallenes with CO. Ligand for the Rh-catalyzed asymmetric enyne cycloisomerization. Catalytic enantioselective addition of dialkylzinc to N-Diphenylphosphinoylimines. Palladium catalyzed asymmetric phosphination. Group: Rhodium series of catalysts. Alternative Names: 210057-23-1; MFCD01862466; 057B231; (-)-1, 2-Bis[ (2R, 5R)-dimethylphospholano]benzene (cyclooCtadiene)rhodium (I) tetrafluoroborate; 1, 2-Bis[ (2R, 5R)-2, 5-dimethylphospholano]benzene (cyclooctadiene)rhodium (I)tetrafluoroborate; (-)-1, 2-Bis ( (2R, 5R)-2, 5-dimethylphospholano)benzene (cyclooctadiene)rhodium (I) tetrafluoroborate; (-)-1, 2-Bis ( (2R, 5R)-2, 5-dimethylphospholano)benzene (cyclooctadiene)rhodium (I) tetrafluoroborate. CAS No. 210057-23-1. Molecular formula: C26H40BF4P2Rh-. Mole weight: 604.263g/mol. IUPAC Name: cycloocta-1, 5-diene; (2R, 5R)-1-[2-[(2R, 5R)-2, 5-dimethylphospholan-1-yl]phenyl]-2, 5-dimethylphospholane; rhodium; tetrafluoroborate. Rotatable Bond Count: 2. Exact Mass: 604.169g/mol. EC Number: 446-280-1. SMILES: [B-](F)(F)(F)F. CC1CCC(P1C2=CC=CC=C2P3C(CCC3C)C)C. C1CC=CCCC=C1. [Rh]. InChI: InChI=1S/C18H28P2.C8H12.BF4.Rh/c1-13-9-10-14(2)19(13)17-7-5-6-8-18(17)20-15(3)11-12-16(20)4;1-2-4-6-8-7-5-3-1;2-1(3,4)5;/h5-8,13-16H,9-12H2,1-4H3;1-2,7-8H,3-6H2;;/q;;-1;/t13-,14-,15-,16-;;;/m1./s1. InChIKey: ZUMNNKGIZSDCBZ-DBMWKRJKSA-N. H-Bond Acceptor: 5. Monoisotopic Mass: 604.169g/mol. | |
(+)-1,2-Bis((2S,5S)-2,5-diethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate, 98+% (S,S)-Et-DUPHOS-Rh Quick inquiry Where to buy Suppliers range | (+)-1,2-Bis((2S,5S)-2,5-diethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate, 98+% (S,S)-Et-DUPHOS-Rh. Uses: The DUPHOS family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. Efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides. Forms superior catalysts for asymmetric reductive aminations. Catalyst used for the asymmetric hydrogenation of enol phosphonates. A novel enantioselective synthesis of β-amino alcohols and 1,2-diamines. Ligand for the catalytic asymmetric [4+1] cycloaddition of vinylallenes with CO. Ligand for the Rh-catalyzed asymmetric enyne cycloisomerization. Catalytic enantioselective addition of dialkylzinc to N-Diphenylphosphinoylimines. Palladium catalyzed asymmetric phosphination. Alternative Names: 1,2-Bis[(2S,5S)-2,5-diethylphospholano]benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate; (+)-1,2-Bis((2S,5S)-2,5-diethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate; AKOS032947597; 1,2-bis[(2S,5S)-2,5-diethyl-phospholano]benzene(1,5-cyclooctadiene)rhodium(I) trifluoromethanesulfonate; MFCD00269861; SC-21592. CAS No. 142184-30-3. Molecular formula: C31H48F3O3P2RhS-. Mole weight: 722.63g/mol. IUPAC Name: (1Z, 5Z)-cycloocta-1, 5-diene; (2S, 5S)-1-[2-[(2S, 5S)-2, 5-diethylphospholan-1-yl]phenyl]-2, 5-diethylphospholane; rhodium; trifluoromethanesulfonate. Rotatable Bond Count: 6. Exact Mass: 722.181g/mol. SMILES: CCC1CCC (P1C2=CC=CC=C2P3C (CCC3CC)CC)CC. C1CC=CCCC=C1. C (F) (F) (F)S (=O) (=O)[O-]. [Rh]. InChI: InChI=1S/C22H36P2. C8H12. CHF3O3S. Rh/c1-5-17-13-14-18(6-2)23(17)21-11-9-10-12-22(21)24-19(7-3)15-16-20(24)8-4; 1-2-4-6-8-7-5-3-1; 2-1(3, 4)8(5, 6)7; /h9-12, 17-20H, 5-8, 13-16H2, 1-4H3; 1-2, 7-8H, 3-6H2; (H, 5, 6, 7); /p-1/b; 2-1-, 8-7-; ; /t17-, 18-, 19-, 20-; ; ; /m0. /s1. InChIKey: XGPXBCKGQLCHDW-ZCTOJWETSA-M. H-Bond Acceptor: 6. Monoisotopic Mass: 722.181g/mol. | |
(+)-1,2-Bis((2S,5S)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (S,S)-Me-DUPHOS-Rh Quick inquiry Where to buy Suppliers range | (+)-1,2-Bis((2S,5S)-2,5-dimethylphospholano)benzene(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, 98+% (S,S)-Me-DUPHOS-Rh. Uses: The DUPHOS family of catalysts is highly efficient for the asymmetric hydrogenation of various substituted acetamidoacrylates and enol acetates yielding products of high enantiomeric excesses. Efficient ligand for the asymmetric hydrogenation of tetrasubstituted enamides. Forms superior catalysts for asymmetric reductive aminations. Catalyst used for the asymmetric hydrogenation of enol phosphonates. A novel enantioselective synthesis of β-amino alcohols and 1,2-diamines. Ligand for the catalytic asymmetric [4+1] cycloaddition of vinylallenes with CO. Ligand for the Rh-catalyzed asymmetric enyne cycloisomerization. Catalytic enantioselective addition of dialkylzinc to N-Diphenylphosphinoylimines. Palladium catalyzed asymmetric phosphination. Group: Rhodium series of catalysts. Alternative Names: (+)-1, 2-Bis ( (2S, 5S)-2, 5-dimethylphospholano)benzene (cyclooctadiene)Rh (I)tetrafluoroborate; (2R,5R)-1-[2-[(2R,5R)-2,5-dimethylphospholan-1-yl]phenyl]-2,5-dimethylphospholane; MFCD01862467; 205064-10-4; AC1MC1E8. CAS No. 205064-10-4. Molecular formula: C26H40BF4P2Rh-. Mole weight: 604.263g/mol. IUPAC Name: cycloocta-1, 5-diene; (2S, 5S)-1-[2-[(2S, 5S)-2, 5-dimethylphospholan-1-yl]phenyl]-2, 5-dimethylphospholane; rhodium; tetrafluoroborate. Rotatable Bond Count: 2. Exact Mass: 604.169g/mol. SMILES: [B-](F)(F)(F)F. CC1CCC(P1C2=CC=CC=C2P3C(CCC3C)C)C. C1CC=CCCC=C1. [Rh]. InChI: InChI=1S/C18H28P2.C8H12.BF4.Rh/c1-13-9-10-14(2)19(13)17-7-5-6-8-18(17)20-15(3)11-12-16(20)4;1-2-4-6-8-7-5-3-1;2-1(3,4)5;/h5-8,13-16H,9-12H2,1-4H3;1-2,7-8H,3-6H2;;/q;;-1;/t13-,14-,15-,16-;;;/m0./s1. InChIKey: ZUMNNKGIZSDCBZ-KXSXXMSISA-N. H-Bond Acceptor: 5. Monoisotopic Mass: 604.169g/mol. | |
[1, 2-Bis (diphenylphosphino) ethane]dichloropalladium (II) Quick inquiry Where to buy Suppliers range | [1, 2-Bis (diphenylphosphino) ethane]dichloropalladium (II). Uses: suzuki reaction. Group: Palladium series catalysts. Alternative Names: Dichloro bis(1,2-diphenylphosphino)ethane-palladium(II); DICHLORO[1,1'-(BIS DIPHENYLPHOSPINO)ETHANE]-PALLADIUM; DICHLORO[1, 2-BIS (DIPHENYLPHOSPHANO)ETHANE]PALLADIUM (II); BCP21886; dichloro (1, 2-bis (diphenylphosphino)ethane)palladium (II); dichloropalladium, 2-diphenylphosphanylethyl (diphenyl)phosphane; AC-4988; PdCl2(dppe); DICHLORO[BIS (1, 2-DIPHENYLPHOSPHINO)ETHANE]PALLADIUM (II); [1,2-Bis(diphenylphosphino)ethane] dichloropalladium(II). CAS No. 19978-61-1. Molecular formula: C26H24Cl2P2Pd. Mole weight: 575.746g/mol. IUPAC Name: dichloropalladium; 2-diphenylphosphanylethyl (diphenyl)phosphane. Rotatable Bond Count: 7. Exact Mass: 573.977g/mol. SMILES: C1=CC=C (C=C1) P (CCP (C2=CC=CC=C2) C3=CC=CC=C3) C4=CC=CC=C4. Cl[Pd]Cl. InChI: InChI=1S/C26H24P2.2ClH.Pd/c1-5-13-23(14-6-1)27(24-15-7-2-8-16-24)21-22-28(25-17-9-3-10-18-25)26-19-11-4-12-20-26;;;/h1-20H,21-22H2;2*1H;/q;;;+2/p-2. InChIKey: LDJXFZUGZASGIW-UHFFFAOYSA-L. Monoisotopic Mass: 573.977g/mol. | |
1,2-bis(diphenylphosphino)ethane palladium dichloride, Pd : 18.5 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: This product is widely used in catalyzing the hydrogenation of olefins, the hydrogenation reduction of nitrobenzene, the oxidation of olefins, the carbonylation of olefins with carbon monoxide, and the coupling of Grignard reagents and halogenated hydrocarbons. Group: Colloidal Catalysts. CAS No. 19978-61-1. Molecular Weight: 575.74 g/mol. SMILES: Cl[Pd]Cl. C (CP (c1ccccc1)c2ccccc2)P (c3ccccc3)c4ccccc4. InChI: LDJXFZUGZASGIW-UHFFFAOYSA-L. Boiling Point: 360 °C. Flash Point: 99 %. | |
1,2-Bis(phenylsulfinyl)ethane palladium(II) acetate Quick inquiry Where to buy Suppliers range | 1,2-Bis(phenylsulfinyl)ethane palladium(II) acetate. Uses: Catalyst for allylic oxidation. Catalyst for oxidative Heck reactions. Catalyst for allylic alkylation. Catalyst for allylic amination. Alternative Names: KS-000013IV; CTK5F5938; 2- (benzenesulfinyl) ethylsulfinylbenzene; 1,2-Bis(phenylsulfinyl)ethane Palladium(II) Diacetate; 858971-43-4; White Catalyst; TR-026796; palladium(2+). CAS No. 858971-43-4. Molecular formula: C18H20O6PdS2. Mole weight: 502.892g/mol. IUPAC Name: 2- (benzenesulfinyl) ethylsulfinylbenzene; palladium (2+) ; diacetate. Rotatable Bond Count: 5. Exact Mass: 501.974g/mol. SMILES: CC (=O)[O-]. CC (=O)[O-]. C1=CC=C (C=C1)S (=O)CCS (=O)C2=CC=CC=C2. [Pd+2]. InChI: InChI=1S/C14H14O2S2.2C2H4O2.Pd/c15-17(13-7-3-1-4-8-13)11-12-18(16)14-9-5-2-6-10-14;2*1-2(3)4;/h1-10H,11-12H2;2*1H3,(H,3,4);/q;;;+2/p-2. InChIKey: SNNYSJNYZJXIFE-UHFFFAOYSA-L. H-Bond Acceptor: 8. Monoisotopic Mass: 501.974g/mol. | |
1, 2-Bis (phenylsulfinyl)ethane Palladium(II) Diacetate Quick inquiry Where to buy Suppliers range | 1, 2-Bis (phenylsulfinyl)ethane Palladium(II) Diacetate. Group: Biochemicals. Alternative Names: White Catalyst. Grades: Highly Purified. CAS No. 858971-43-4. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane Quick inquiry Where to buy Suppliers range | 1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane. Uses: A bulky, robust, and electron-poor ligand that gives efficient rhodium hydroformylation and palladium cross-coupling catalysts. Alternative Names: 1,3,5,7-Tetramethyl-8-phenyl-2,4,6-trioxa-8-phosphatricyclo[3.3.1.13,7]decane; 1,3,5,7-Tetramethyl-6-phenyl-2,4,8-trioxa-6-phosphaadamantane, 99%; 97739-46-3; CTK5H9495; 1,3,5,7-TETRAMETHYL-6-PHENYL-2,4,8-TRIOXA-6-PHOSPHAADAMANTANE; DTXSID50699640; AVVSJWUWBATQBX-UHFFFAOYSA-N; KS-000018KV; 1,3,5,7-tetramethyl-2,4,8-trioxa-6-phospha-adamantane; MFCD10567051. CAS No. 97739-46-3. Molecular formula: C16H21O3P. Mole weight: 292.315g/mol. IUPAC Name: 1,3,5,7-tetramethyl-8-phenyl-2,4,6-trioxa-8-phosphatricyclo[3.3.1.13,7]decane. Rotatable Bond Count: 1. Exact Mass: 292.123g/mol. SMILES: CC12CC3 (OC (O1) (CC (O2) (P3C4=CC=CC=C4)C)C)C. InChI: InChI=1S/C16H21O3P/c1-13-10-15(3)19-14(2,17-13)11-16(4,18-13)20(15)12-8-6-5-7-9-12/h5-9H,10-11H2,1-4H3. InChIKey: AVVSJWUWBATQBX-UHFFFAOYSA-N. H-Bond Acceptor: 3. Monoisotopic Mass: 292.123g/mol. | |
[1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene][1,3-divinyl-1,1,3,3-tetramethyldisiloxane]palladium(0) Quick inquiry Where to buy Suppliers range | [1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene][1,3-divinyl-1,1,3,3-tetramethyldisiloxane]palladium(0). Uses: Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Telomerization. Group: Catalysts for Pharmaceutical. CAS No. 441018-46-8. Molecular Weight: 597.26. Molecular Formula: C29H42N2OSi2Pd. Purity: Metal purity 99.95. | |
1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (1,4-naphthoquinone)palladium(0) dimer Quick inquiry Where to buy Suppliers range | 1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (1,4-naphthoquinone)palladium(0) dimer. Uses: Catalyst for Heck reactions in ionic liquids. Catalyst for the cross-coupling of aryl diazonium salts. Catalyst for the Kumada cross-coupling of alkyl chlorides. Group: Heterocyclic Organic Compound. Alternative Names: Naphthoquinone-1,3-bis(2,4,6-trimethylphenyl)-imidazole-2-ylidenepalladium(0), CX 12; 1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene (1,4-naphthoquinone)palladium(0) dimer; UMICORE CX12; NAPHTHOQUINONE[1,3-BIS(MESITYL)IMIDAZOLE-2-YLIDENE]PALLADIUM(0); MFCD08705778; 1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene(1,4-naphthoquinone)palladium(0) dimer; Bis[1,3-dihydro-1,3-(2,4,6-trimethylphenyl)-2H-imidazol-2-ylidene]bis[|I-[(2,3-|C)-1,4-naphthalenedione-|EO]]di-palladium, CX 12. CAS No. 467220-49-1. Molecular formula: C62H60N4O4Pd2. Mole weight: 1138.026g/mol. IUPAC Name: [1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium;naphthalene-1,4-dione. Rotatable Bond Count: 4. Exact Mass: 1138.269g/mol. SMILES: CC1=CC (=C (C (=C1)C)N2C=CN (C2=[Pd])C3=C (C=C (C=C3C)C)C)C. CC1=CC (=C (C (=C1)C)N2C=CN (C2=[Pd])C3=C (C=C (C=C3C)C)C)C. C1=CC=C2C (=O)C=CC (=O)C2=C1. C1=CC=C2C (=O)C=CC (=O)C2=C1. InChI: InChI=1S/2C21H24N2.2C10H6O2.2Pd/c2*1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6;2*11-9-5-6-10(12)8-4-2-1-3-7(8)9;;/h2*7-12H,1-6H3;2*1-6H;; InChIKey: ZTBFODSKEBBIJJ-UHFFFAOYSA-N. H-Bond Acceptor: 8. Monoisotopic Mass: 1136.268g/mol. | |
1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene, min. 98% Quick inquiry Where to buy Suppliers range | 1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene, min. 98%. Uses: Nucleophilic carbene that serves as a bulky, electron-rich "phosphine mimic" for metal-catalyzed reactions. (a) Palladium-catalyzed Suzuki cross-coupling of aryl chlorides. (b) Ruthenium-carbene complexes serve as more reactive catalyst for ring-closing metathesis. Alternative Names: IMes; 141556-42-5; D3870; C-1996; 1,3-BIS(2,4,6-TRIMETHYLPHENYL)IMIDAZOL-2-YLIDENE; 6880AA; SC11699; 1,3-Dimesitylimidazol-2-ylidene; AK119064; 1,3-bis(2,4,6-trimethylphenyl)-imidazolium. CAS No. 141556-42-5. Molecular formula: C21H24N2. Mole weight: 304.437g/mol. IUPAC Name: 1,3-bis(2,4,6-trimethylphenyl)-2H-imidazol-1-ium-2-ide. Rotatable Bond Count: 2. Exact Mass: 304.194g/mol. SMILES: CC1=CC(=C(C(=C1)C)N2C=C[N+](=[C-]2)C3=C(C=C(C=C3C)C)C)C. InChI: InChI=1S/C21H24N2/c1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6/h7-12H,1-6H3. InChIKey: JCYWCSGERIELPG-UHFFFAOYSA-N. H-Bond Acceptor: 1. Monoisotopic Mass: 304.194g/mol. | |
1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidene(1,4-naphthoquinone)palladium(0) dimer, 96% Quick inquiry Where to buy Suppliers range | 1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidene(1,4-naphthoquinone)palladium(0) dimer, 96%. Uses: Catalyst for Heck reactions in ionic liquids. Catalyst for the cross-coupling of aryl diazonium salts. Catalyst for the Kumada cross-coupling of alkyl chlorides. CAS No. 649736-75-4. Molecular formula: C74H84N4O4Pd2. Mole weight: 1306.3. | |
[1,3-Bis(2,6-di-isopropylphenyl)-4,5-dihydroimidazol-2-ylidene]chloro][3-phenylallyl]palladium(II) Quick inquiry Where to buy Suppliers range | [1,3-Bis(2,6-di-isopropylphenyl)-4,5-dihydroimidazol-2-ylidene]chloro][3-phenylallyl]palladium(II). Uses: Catalyst used for the room temperature Buchwald-Hartwig amination of hindered aryl chlorides. CAS No. 884879-24-7. Mole weight: 649.64. | |
1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate Quick inquiry Where to buy Suppliers range | 1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate. Uses: In-situ deprotonation leads to metal carbene species which acts as a catalyst in a variety of C-C and C-N bond forming reactions. Ligand used in the nickel or palladium-catalyzed coupling of aryl chlorides and amines. Ligand used for the palladium-catalyzed arylation of esters and amides. Ligand used for the palladium-catalyzed intermolecular amination of Csp3-H Bonds. Ligand used for the nickel-catalyzed hydrogenation of olefins. Group: Organic Phosphine Compounds. Alternative Names: DTXSID60463955; CTK1A1650; AN-29083; 1,3-Bis-(2,6-diisopropylphenyl)imidazolinium tetrafluoroborate; SC11685; SIPr.HBF4; AKOS015832942; SIPr-HBF4; I14-3250; 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dihydroimidazol-1-ium,tetrafluoroborate. CAS No. 282109-83-5. Molecular formula: C27H39BF4N2. Mole weight: 478.427g/mol. IUPAC Name: 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dihydroimidazol-1-ium;tetrafluoroborate. Rotatable Bond Count: 6. Exact Mass: 478.314g/mol. SMILES: [B-] (F) (F) (F)F. CC (C)C1=C (C (=CC=C1)C (C)C)N2CC[N+] (=C2)C3=C (C=CC=C3C (C)C)C (C)C. InChI: InChI=1S/C27H39N2.BF4/c1-18(2)22-11-9-12-23(19(3)4)26(22)28-15-16-29(17-28)27-24(20(5)6)13-10-14-25(27)21(7)8;2-1(3,4)5/h9-14,17-21H,15-16H2,1-8H3;/q+1;-1. InChIKey: KFZBJQUHHALFSR-UHFFFAOYSA-N. H-Bond Acceptor: 5. Monoisotopic Mass: 478.314g/mol. | |
[1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene][1,3-divinyl-1,1,3,3-tetramethyldisiloxane]palladium(0) Quick inquiry Where to buy Suppliers range | [1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene][1,3-divinyl-1,1,3,3-tetramethyldisiloxane]palladium(0). Uses: Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Telomerization. Group: Catalysts for Pharmaceutical. CAS No. 478019-87-3. Molecular Weight: 681.42. Molecular Formula: C35H54N2OSi2Pd. Purity: Metal purity 99.95. | |
[1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloro[3-phenylallyl]palladium(II) Quick inquiry Where to buy Suppliers range | yellow powder or crystals. Uses: Catalyst used for room temperature Suzuki-Miyaura couplings. Catalyst used for rapid, room temperature Buchwald-Hartwig and Suzuki-Miyaura coupling reactions. Group: Palladium series catalysts. Alternative Names: CX 31. CAS No. 884879-23-6. Molecular formula: C36H45ClN2Pd. Mole weight: 647.63. Symbol: GHS07. Melting Point: 205-208 °C. Safty Description: Warning. Hazard statements: H302-H312-H315-H319-H332. | |
(1, 3-Bis (diphenylphosphino)propane)palladium (II) chloride Quick inquiry Where to buy Suppliers range | (1, 3-Bis (diphenylphosphino)propane)palladium (II) chloride. Uses: suzuki reaction. Group: Palladium series catalysts. Alternative Names: A832490; C27H26Cl2P2Pd; AB1007454; PD(DPPP)CL2; dichloro-[1, 3bis (diphenylphosphino)propane]palladium (ii); 1, 3-bis (diphenylphosino)propane)palladium (II)dichloride; [1, 3-BIS (DIPHENYLPHOSPHINO) PROPANE]DICHLOROPALLADIUM (II) ; 831D026; pdcl2(dppp); dichloro (1, 3-bis (diphenylphosphino)propane)palladium (ii). CAS No. 59831-02-6. Molecular formula: C27H26Cl2P2Pd. Mole weight: 589.773g/mol. IUPAC Name: dichloropalladium; 3-diphenylphosphanylpropyl (diphenyl)phosphane. Rotatable Bond Count: 8. Exact Mass: 587.992g/mol. SMILES: C1=CC=C (C=C1) P (CCCP (C2=CC=CC=C2) C3=CC=CC=C3) C4=CC=CC=C4. Cl[Pd]Cl. InChI: InChI=1S/C27H26P2.2ClH.Pd/c1-5-14-24(15-6-1)28(25-16-7-2-8-17-25)22-13-23-29(26-18-9-3-10-19-26)27-20-11-4-12-21-27;;;/h1-12,14-21H,13,22-23H2;2*1H;/q;;;+2/p-2. InChIKey: LDFBXJODFADZBN-UHFFFAOYSA-L. Monoisotopic Mass: 587.992g/mol. | |
(1, 3-Divinyl-1, 1, 3, 3-tetramethyldisiloxane) [1, 1'-bis (diisopropylphosphino) ferrocene]palladium (0) toluene solution Quick inquiry Where to buy Suppliers range | (1, 3-Divinyl-1, 1, 3, 3-tetramethyldisiloxane) [1, 1'-bis (diisopropylphosphino) ferrocene]palladium (0) toluene solution. Uses: Amination?Buchwald-Hartwig Aminaton. Group: Catalysts for Pharmaceutical; Amination. CAS No. 1708984-17-1. Molecular Weight: 711.13. Molecular Formula: C30H54FeOP2PdSi2. Purity: Metal purity 99.95. | |
1,4-Bis(diphenylphosphino)butane-palladium(II) chloride Quick inquiry Where to buy Suppliers range | 1,4-Bis(diphenylphosphino)butane-palladium(II) chloride. Uses: Catalyst for the Grignard coupling for regioand stereoselective monoalkylation and arylation of 1,1-dichloro-1-alkenes Synthetic pyrethriods: catalyst for the Negishi coupling of (2, 2-dihaloethenyl) cyclopropanecarboxylates. Group: Palladium series catalysts. Alternative Names: 1,4-Bis(diphenylphosphino)butane-palladium(II)chloride; 29964-62-3; 1,4-BIS(DIPHENYLPHOSPHINE)BUTANE PALLADIUM(II) CHLORIDE; JQXJBXVWVPVTOO-UHFFFAOYSA-L; 1,4-Bis(diphenylphosphine)butane palladium(II)chloride; 1,4-Bis(diphenylphosphino)butane-palladium(II) chloride, >=95.0%; 1,4-bis(diphenylphosphino)butane palladium(II) dichloride; DB-050506; [1, 4-bis (diphenylphosphino)butane]palladium (ii)dichloride; PALLADIUM(II)CHLORIDE-1,4-BIS(DIPHENYLPHOSPHINE)BUTANE. CAS No. 29964-62-3. Molecular formula: C28H28Cl2P2Pd. Mole weight: 603.8g/mol. IUPAC Name: dichloropalladium; 4-diphenylphosphanylbutyl (diphenyl)phosphane. Rotatable Bond Count: 9. Exact Mass: 602.008g/mol. SMILES: C1=CC=C (C=C1) P (CCCCP (C2=CC=CC=C2) C3=CC=CC=C3) C4=CC=CC=C4. Cl[Pd]Cl. InChI: InChI=1S/C28H28P2.2ClH.Pd/c1-5-15-25(16-6-1)29(26-17-7-2-8-18-26)23-13-14-24-30(27-19-9-3-10-20-27)28-21-11-4-12-22-28;;;/h1-12,15-22H,13-14,23-24H2;2*1H;/q;;;+2/p-2. InChIKey: JQXJBXVWVPVTOO-UHFFFAOYSA-L. Monoisotopic Mass: 602.008g/mol. | |
(1,5-Cyclooctadiene)iridium(I) chloride dimer, 97 % Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·For hydrogenation, allyl alkylation, allyl amination, cycloaddition and other reactions; ·The raw material for the synthesis of various iridium compounds. Group: Colloidal Catalysts. CAS No. 12112-67-3. Molecular Weight: 671.7 g/mol. SMILES: Cl[Ir]. Cl[Ir]. C1CC=CCCC=C1. C2CC=CCCC=C2. InChI: ZFOUDQNHNLDNLD-MIXQCLKLSA-L. Boiling Point: 205 °C (dec.) (lit.). Flash Point: 97 %. | |
(1,5-Cyclooctadiene)iridium(I) chloride dimer, 98 % Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·For hydrogenation, allyl alkylation, allyl amination, cycloaddition and other reactions; ·The raw material for the synthesis of various iridium compounds. Group: Colloidal Catalysts. CAS No. 12112-67-3. Molecular Weight: 671.7 g/mol. SMILES: Cl[Ir]. Cl[Ir]. C1CC=CCCC=C1. C2CC=CCCC=C2. InChI: ZFOUDQNHNLDNLD-MIXQCLKLSA-L. Boiling Point: 205 °C (dec.) (lit.). Flash Point: 98 %. | |
(1,5-Cyclooctadiene)(μ-methoxy)iridium(I) Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·Coupling, hydroboration, carbon-hydrogen bond activation reactions; ·Preparation of heteroaryl-fused indole ring systems; ·For the synthesis of biaryl and heterobiaryl compounds; ·As an inhibitor of HCV NS5B polymerase. Group: Colloidal Catalysts. CAS No. 12148-71-9. Molecular Weight: 662.86 g/mol. SMILES: C[O+]1[Ir-]2[O+](C)[Ir-]12.C3CC=CCCC=C3.C4CC=CCCC=C4. InChI: BGWIAAATAAWGOI-MIXQCLKLSA-N. Boiling Point: 154-179 °C (D). Flash Point: 96 %. | |
(1,5-cyclooctadiene)palladium(II) chloride, Pd : 34.9 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: Catalysts for C-C and C-N bond formation for Heck coupling of alkynes with alkenes, Suzuki coupling of aryl bromides, allylic substitution of oximes with allyl esters, and methoxycarbonyl of iodobenzene reaction. Group: Colloidal Catalysts. CAS No. 12107-56-1. Molecular Weight: 285.51 g/mol. SMILES: Cl[Pd]Cl.C1CC=CCCC=C1. InChI: RRHPTXZOMDSKRS-PHFPKPIQSA-L. Boiling Point: 210 °C (dec.) (lit.). Flash Point: 99 %. Density: Soluble in dichloromethane. | |
(1,5-cyclooctadiene) palladium(II) dichloride, Pd : 37.3 % Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: Catalysts for C-C and C-N bond formation for Heck coupling of alkynes with alkenes, Suzuki coupling of aryl bromides, allylic substitution of oximes with allyl esters, and methoxycarbonyl of iodobenzene reaction. Group: Colloidal Catalysts. CAS No. 12107-56-1. Molecular Weight: 285.51 g/mol. SMILES: Cl[Pd]Cl.C1CC=CCCC=C1. InChI: RRHPTXZOMDSKRS-PHFPKPIQSA-L. Boiling Point: 210 °C (dec.) (lit.). Flash Point: 99 %. Density: Soluble in dichloromethane. | |
(1,5-Cyclooctadiene)rhodium(I) chloride dimer Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·Catalysts for the coupling of 1,3-dienes with activated hydrocarbons and the preparation of chiral complexing agents; ·Rhodium-catalyzed oxidative addition to terminal alkynes to synthesize esters, amides and carboxylic acids; ·Efficient and selective catalysts for asymmetric synthesis. Group: Colloidal Catalysts. CAS No. 12092-47-6. Molecular Weight: 493.08 g/mol. SMILES: Cl[Rh]. Cl[Rh]. C1CC=CCCC=C1. C2CC=CCCC=C2. InChI: QSUDXYGZLAJAQU-MIXQCLKLSA-L. Boiling Point: 243 °C (dec.) (lit.). Flash Point: 98 %. | |
1-Bromo-2-methoxy-naphthalene Quick inquiry Where to buy Suppliers range | 1-Bromo-2-methoxy-naphthalene is a useful synthetic intermediate. It is used as a reagent to syntheisze a catalyst for highly enantioselective aziridination of styrene derivatives. It can also be used to prepare biaryls or biheterocycles by palladium-catalyzed Ullmann coupling. Group: Biochemicals. Grades: Highly Purified. CAS No. 3401-47-6. Pack Sizes: 5g, 25g. Molecular Formula: C11H9BrO, Molecular Weight: 237.09. US Biological Life Sciences. | Worldwide |
1-Diphenylphosphino-1?-(di-tert-butylphosphino)ferrocene Quick inquiry Where to buy Suppliers range | 1-Diphenylphosphino-1?-(di-tert-butylphosphino)ferrocene. Uses: Catalyst in microwave-assisted preparation of aryl-alkyl ethers via palladium-catalyzed Hiyama coupling of alkoxysilanes with aryl bromides or aryl chlorides Ligand for catalytic isomerization of methylbutenenitrile via nickel systems Ligand for ruthenium alkylidene complexes for catalysis of metathesis reactions and catalytic norbornene polymerization. Alternative Names: 95408-38-1;DTXSID00746613;Ferrocene, 1-[bis(1,1-dimethylethyl)phosphino]-1'-(diphenylphosphino)-;1-Diphenylphosphino-1 inverted exclamation marka-(di-tert-butylphosphino)ferrocene;Iron(2+) 1-(di-tert-butylphosphanyl)cyclopenta-2,4-dien-1-ide 1-(diphenylphosphanyl)cyclopenta-2,4-dien-1-ide (1/1/1). CAS No. 95408-38-1. Molecular formula: C30H36FeP2. Mole weight: 514.411g/mol. IUPAC Name: cyclopenta-1,4-dien-1-yl(diphenyl)phosphane;ditert-butyl(cyclopenta-1,4-dien-1-yl)phosphane;iron(2+). Rotatable Bond Count: 6. Exact Mass: 514.164g/mol. SMILES: CC (C) (C)P (C1=C[CH-]C=C1)C (C) (C)C. [CH-]1C=CC (=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Fe+2]. InChI: InChI=1S/C17H14P.C13H22P.Fe/c1-3-9-15(10-4-1)18(17-13-7-8-14-17)16-11-5-2-6-12-16;1-12(2,3)14(13(4,5)6)11-9-7-8-10-11;/h1-14H;7-10H,1-6H3;/q2*-1;+2. InChIKey: KVXWCDXJSYVISP-UHFFFAOYSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 514.164g/mol. | |
(1E,2E)-1,2-Bis(2,6-Diisopropylphenylimino)ethane Quick inquiry Where to buy Suppliers range | (1E,2E)-1,2-Bis(2,6-Diisopropylphenylimino)ethane. Uses: Reactant in preparation of derived ruthenium olefin metathesis catalysts 1 N-cyclic carbene ligand 2 Catalyst in: Palladium-catalyzed aerobic alc. oxidn. supported by a-diimine ligands 3 Regioselective alkylation in presence of ruthenium-bisimine catalytic precursors 4 N-arylation of aromatic amines 5 Preparation of ruthenium nitrosyl alpha-diimine and iminoketone complexes as catalysts for transfer hydrogenation of ketones and atom transfer radical polymerization reactions. Alternative Names: N,N'-Bis(2,6-diisopropylphenyl)ethanediimine; AKOS004909627; 1,2-bis(2,6-diisopropylphenylimino)ethane; RL04839; AKOS030229349; ZINC252616095; Glyoxal bis(2,6-diisopropylanil); J-502081; AJ-63795; (1E,2E)-N1,N2-bis[2,6-bis(propan-2-yl)phenyl]ethane-1,2-diimine. CAS No. 74663-75-5. Molecular formula: C26H36N2. Mole weight: 376.588g/mol. IUPAC Name: N,N'-bis[2,6-di(propan-2-yl)phenyl]ethane-1,2-diimine. Rotatable Bond Count: 7. Exact Mass: 376.288g/mol. SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N=CC=NC2=C (C=CC=C2C (C)C)C (C)C. InChI: InChI=1S/C26H36N2/c1-17(2)21-11-9-12-22(18(3)4)25(21)27-15-16-28-26-23(19(5)6)13-10-14-24(26)20(7)8/h9-20H,1-8H3. InChIKey: JWVIIGXMTONOFR-UHFFFAOYSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 376.288g/mol. | |
(2,2?-Bipyridine)dichloropalladium(II) Quick inquiry Where to buy Suppliers range | (2,2?-Bipyridine)dichloropalladium(II). Group: Palladium series catalysts. Alternative Names: 2-pyridin-2-ylpyridine; 2,2'-Bipyridine-dichloropalladium (1:1); Bis(2,2 inverted exclamation marka-Bipyridine)palladium dichloride; Dichloro(2,2 inverted exclamation marka-bipyridine)palladium; KS-00000VHX; TRA0034672; BIS(2,2'-BIPYRIDINE)PALLADIUM DICHLORIDE; 2,2'-BIPYRIDYLPALLADIUM DICHLORIDE; AM84940; 2,2 inverted exclamation marka-Bipyridylpalladium dichloride. CAS No. 14871-92-2. Molecular formula: C10H8Cl2N2Pd. Mole weight: 333.508g/mol. IUPAC Name: dichloropalladium;2-pyridin-2-ylpyridine. Rotatable Bond Count: 1. Exact Mass: 331.91g/mol. SMILES: C1=CC=NC(=C1)C2=CC=CC=N2.Cl[Pd]Cl. InChI: InChI=1S/C10H8N2.2ClH.Pd/c1-3-7-11-9(5-1)10-6-2-4-8-12-10;;;/h1-8H;2*1H;/q;;;+2/p-2. InChIKey: MUNARLQNCCGPQU-UHFFFAOYSA-L. H-Bond Acceptor: 2. Monoisotopic Mass: 331.91g/mol. | |
2,5-Dimethyl-1,1'-biphenyl Quick inquiry Where to buy Suppliers range | 2,5-Dimethyl-1,1'-biphenyl is a useful reagent for organic synthesis. It is used in the preparation of orthopalladated phosphorus ylide complexes and palladium nanoparticles as catalyst for Suzuki coupling reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 7372-85-2. Pack Sizes: 100mg, 500mg. Molecular Formula: C14H14, Molecular Weight: 182.26. US Biological Life Sciences. | Worldwide |
[2-(5-Methyl-1H-pyrazol-3-yl-κN2)pyridinato-κN](η3-2-propenyl)palladium Tetrafluoroborate Quick inquiry Where to buy Suppliers range | [2-(5-Methyl-1H-pyrazol-3-yl-κN2)pyridinato-κN](η3-2-propenyl)palladium Tetrafluoroborate is an coordination complex used as an catalyst in he synthesis of cyclopropanation of ketene silyl acetal with allylic acetates. Group: Biochemicals. Grades: Highly Purified. CAS No. 215323-63-0. Pack Sizes: 10mg, 100mg. Molecular Formula: C12H12BF4N3Pd. US Biological Life Sciences. | Worldwide |
[2, 6-Bis[ (di-1-piperidinylphosphino) amino]phenyl]palladium (II) chloride Quick inquiry Where to buy Suppliers range | [2, 6-Bis[ (di-1-piperidinylphosphino) amino]phenyl]palladium (II) chloride. Group: Palladium series catalysts. Alternative Names: (2, 6-Bis ( (di (piperidin-1-yl)phosphino)amino)phenyl)palladium (II) chloride;955035-37-7;MFCD17019351;AKOS016012103;KS-00000R52;AK122621. CAS No. 955035-37-7. Molecular formula: C26H45ClN6P2Pd. Mole weight: 645.506g/mol. IUPAC Name: 1-N,3-N-bis[di(piperidin-1-yl)phosphanyl]benzene-2-ide-1,3-diamine;palladium(2+);chloride. Rotatable Bond Count: 8. Exact Mass: 644.19g/mol. SMILES: C1CCN (CC1)P (NC2=[C-]C (=CC=C2)NP (N3CCCCC3)N4CCCCC4)N5CCCCC5. [Cl-]. [Pd+2]. InChI: InChI=1S/C26H45N6P2.ClH.Pd/c1-5-16-29(17-6-1)33(30-18-7-2-8-19-30)27-25-14-13-15-26(24-25)28-34(31-20-9-3-10-21-31)32-22-11-4-12-23-32;;/h13-15,27-28H,1-12,16-23H2;1H;/q-1;;+2/p-1. InChIKey: XASCRSOQTJTSCW-UHFFFAOYSA-M. H-Bond Donor: 2. H-Bond Acceptor: 8. Monoisotopic Mass: 644.19g/mol. | |
2,6-Dimethylbiphenyl Quick inquiry Where to buy Suppliers range | 2,6-Dimethylbiphenyl acts as a reagent in the preparation of palladium catalyst for Suzuki-Miyaura cross-coupling reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 3976-34-9. Pack Sizes: 50mg, 100mg. Molecular Formula: C14H14, Molecular Weight: 182.26. US Biological Life Sciences. | Worldwide |
2-[Bis(2,4-di-tert-butyl-phenoxy)phosphinooxy]-3,5-di(tert-butyl)phenyl-palladium(II) chloride dimer Quick inquiry Where to buy Suppliers range | 2-[Bis(2,4-di-tert-butyl-phenoxy)phosphinooxy]-3,5-di(tert-butyl)phenyl-palladium(II) chloride dimer. Group: Palladium Complexes. Alternative Names: Bedford catalyst. Grades: 99%. CAS No. 217189-40-7. Product ID: ACM217189407-1. Molecular formula: C84H126Cl2O6P2Pd2. Mole weight: 1577.6. Appearance: White like powder. SMILES: CC (C) (C)C1=CC (=C (C=C1)OP (OC2=C (C=C (C=C2)C (C) (C)C)C (C) (C)C)OC3=C (C=C (C=[C-]3)C (C) (C)C)C (C) (C)C)C (C) (C)C. CC (C) (C)C1=CC (=C (C=C1)OP (OC2=C (C=C (C=C2)C (C) (C)C)C (C) (C)C)OC3=C (C=C (C=[C-]3)C (C) (C)C)C (C) (C)C)C (C) (C)C. [ClH+][Pd][ClH+]. [Pd]. | |
2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl Quick inquiry Where to buy Suppliers range | 2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl. Uses: Exceptional ligands for Pd-catalyzed amination and amidation of aryl sulfonates. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling reaction and carbonyl enolate coupling. Ligand used for the chemoselective amination of aryl chlorides. Ligand used for the Pd-catalyzed borylation of aryl chlorides, for the formation of trifluoroborates. Ligand used for the Pd-catalyzed amination of vinyl halides and triflates. Ligand used for the Pd-catalyzed three-component synthesis of indoles. Ligand used for the Pt-catalyzed regioselective hydrosilylation of functionalized terminal arylalkynes. Ligand used for the Pd-catalyzed synthesis of carbazoles. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling of aryl chloride and NHC-boranes. Ligand used for the direct arylation of picoline N-oxide. Ligand used for the Negishi coupling of 2-heterocyclic organozinc reagents. Catalyst for a phosphine-catalyzed Heine reaction. Ligand used for the palladium-catalyzed oxidative coupling of indoles and heteroarenes. Ligand used for the silver-catalyzed hydrogenation of aldehydes. Ligand used for the palladium-catalyzed cyanation of heterycyclic halides. Group: Organic Phosphine Compounds. Alternative Names: dicyclohexyl[2-(2,4,6-triisopropylphenyl)phenyl]phosphane; ING0003480; 2,4,6-triisopropyl-2'-(dicyclohexylphosphino)biphenyl; X7076; 2-dicyclohexylphosphino-2',4',6'-triisopropyl-1,1' biphenyl; 100122-EP2289877A1; X-Phos; dicyclohexyl[2',4',6'-tris(propan-2-yl)-[1,1'-biphenyl]-2-yl]phosphane; AC-1757; 2-(dicyclohexylphosphino)-2',4',6'-triisopropyl-biphenyl. CAS No. 564483-18-7. Molecular formula: C33H49P. Mole weight: 476.729g/mol. IUPAC Name: dicyclohexyl-[2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Rotatable Bond Count: 7. Exact Mass: 476.357g/mol. SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=CC=CC=C2P (C3CCCCC3)C4CCCCC4)C (C)C. InChI: InChI=1S/C33H49P/c1-23(2)26-21-30(24(3)4)33(31(22-26)25(5)6)29-19-13-14-20-32(29)34(27-15-9-7-10-16-27)28-17-11-8-12-18-28/h13-14,19-25,27-28H,7-12,15-18H2,1-6H3. InChIKey: UGOMMVLRQDMAQQ-UHFFFAOYSA-N. Monoisotopic Mass: 476.357g/mol. | |
2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl Quick inquiry Where to buy Suppliers range | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl. Uses: Ligand/palladium catalyst for general Suzuki-Miyaura cross-coupling reactions. Ligand/palladium catalyst for the Suzuki-Miyaura coupling of aryltrifluoroborates with aryl chlorides. Ligand/palladium catalyst for the Suzuki-Miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters. Ligand/palladium catalyst for the Kumada-Corriu cross-coupling reaction. Ligand/palladium catalyst for the borylation of aryl halides with pinacol borane. Suzuki couplings involving amino acids. Synthesis of biaryl derivatives of 4-hydroxyphenyl glycine, tyrosine and tryptophan. Synthesis of substituted adamantylzinc reagents using Mg-insertion in the presence of zinc chloride. Highly efficient catalyst for the palladium-catalyzed Suzuki-Miyura reaction of heteroaryl halides and heteroaryl boronic acids and esters. Group: Organic Phosphine Compounds. Alternative Names: ANW-35081; 2-Dicyclohexylphosphino-2 inverted exclamation mark ,6 inverted exclamation mark -dimethoxybiphenyl; 2-(dicyclohexylphosphino)-2', 6'-dimethoxybiphenyl; [2',6'-bis(methyloxy)-2-biphenylyl](dicyclohexyl)phosphane; 2-Dicyclohexylphosphino-2 ,6 -dimethoxybiphenyl; RL04508; 2-Dicyclohexylphoshino-2',6'-dimethoxy-1,1'-biphenyl; 2-(dicyclohexylphosphino)-2',6'-dimethoxy-1,1'-biphenyl; AN-11453; 2,6-dimethoxy-2' (dicyclohexylphosphino)biphenyl. CAS No. 657408-07-6. Molecular formula: C26H35O2P. Mole weight: 410.538g/mol. IUPAC Name: dicyclohexyl-[2-(2,6-dimethoxyphenyl)phenyl]phosphane. Rotatable Bond Count: 6. Exact Mass: 410.237g/mol. SMILES: COC1=C (C (=CC=C1)OC)C2=CC=CC=C2P (C3CCCCC3)C4CCCCC4. InChI: InChI=1S/C26H35O2P/c1-27-23-17-11-18-24(28-2)26(23)22-16-9-10-19-25(22)29(20-12-5-3-6-13-20)21-14-7-4-8-15-21/h9-11,16-21H,3-8,12-15H2,1-2H3. InChIKey: VNFWTIYUKDMAOP-UHFFFAOYSA-N. H-Bond Acceptor: 2. Monoisotopic Mass: 410.237g/mol. | |
2?-(Dimethylamino)-2-biphenylyl-palladium(II) chloride Dinorbornylphosphine complex Quick inquiry Where to buy Suppliers range | 2?-(Dimethylamino)-2-biphenylyl-palladium(II) chloride Dinorbornylphosphine complex. Uses: A new, air and moisture-stable, palladium catalyst useful in a broad scope of C-C and C-N coupling reactions. The highlyactive catalyst can tolerate substrates containing a wide variety of functional groups such as alkyls, alkoxides, ketones, aldehydes, esters, amines, trifluoromethyl and nitro groups. Group: Heterocyclic Organic Compound. Alternative Names: MFCD03427335; YMZCYRNVJBOOCT-MUGRSZJDSA-M; chloro[2'-(dimethylamino)-2-biphenylyl]palladium (1R,4S)-bicyclo[2.2.1]hept-2-yl[(1S,4R)-bicyclo[2.2.1]hept-2-yl]phosphane; 2'-(Dimethylamino)-2-biphenylyl-palladium(II) chloride Dinorbornylphosphine complex, >=99.0% (C); chloro[2'-(dimethylamino)-2-biphenylyl]palladium 1(1R,4S)-bicyclo[2.2.1]hept-2-yl[(1S,4R)-bicyclo[2.2.1 ]hept-2-yl]phosphane; 2 inverted exclamation marka-(Dimethylamino)-2-biphenylyl-palladium(II) chloride Dinorbornylphosphine complex; chloro[2'-(dimethylamino)-2-biphenylyl]palladium 1(1R,4S)-bicyclo[2.2.1]hept-2-yl[(1S,4R)-bicyclo[2.2.1]hept-2-yl]phosphane. CAS No. 359803-53-5. Molecular formula: C28H37ClNPPd. Mole weight: 560.455g/mol. IUPAC Name: [(1S, 4R)-2-bicyclo[2.2.1]heptanyl]-[(1R, 4S)-2-bicyclo[2.2.1]heptanyl]phosphane; chloropalladium(1+); N, N-dimethyl-2-phenylaniline. Rotatable Bond Count: 4. Exact Mass: 559.139g/mol. SMILES: CN(C)C1=CC=CC=C1C2=CC=CC=[C-]2.C1CC2CC1CC2PC3CC4CCC3C4.Cl[Pd+]. InChI: InChI=1S/C14H14N.C14H23P.ClH.Pd/c1-15(2)14-11-7-6-10-13(14)12-8-4-3-5-9-12;1-3-11-5-9(1)7-13(11)15-14-8-10-2-4-12(14)6-10;;/h3-8,10-11H,1-2H3;9-15H,1-8H2;1H;/q-1;;;+2/p-1/t;9-,10+,11+,12-,13 ,14 ,15 ;; InChIKey: JZMMCQBNMQSWGC-MUGRSZJDSA-M. H-Bond Acceptor: 2. Monoisotopic Mass: 559.139g/mol. | |
2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride Dinorbornylphosphine Complex Quick inquiry Where to buy Suppliers range | 2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride Dinorbornylphosphine Complex. Uses: Efficient catalyst for the amination of aryl chlorides Catalyst used for the efficient synthesis of substituted biaryl anilines and biaryl phenols. Catalyst used for the direct vinylation, and difluorovinylation, of arylboronic acids. Catalyst used in the Heck coupling of vinyl phosphates. CAS No. 614753-51-4. Mole weight: 606.30. | |
2-(Di-tert-Butylphosphino)biphenyl Quick inquiry Where to buy Suppliers range | 2-(Di-tert-Butylphosphino)biphenyl. Uses: Ligand used in the palladium-catalyzed synthesis of aromatic amines from aryl chlorides, bromides and triflates. Ligand employed in a very active and general catalyst for Suzuki coupling reactions using aryl chlorides, bromides and triflates. Ligand used in palladium-catalyzed synthesis of oxindoles from α-chloroacetanilides. Effective ligand used in palladium-catalyzed arylation of thiazoles. Used in the formation of 2-benzylindolines via sequential palladium-catalyzed N-arylation/cyclization/C-arylation. Selective in the palladium-catalyzed arylation of silyl enol ethers formed from copper-catalyzed reduction of enones. Group: Organic Phosphine Compounds. Alternative Names: 4CH-015688; AC-4975; 2-(di-tert-butyl-phosphino)biphenyl; Buchwald phosphine ligands, johnphos phosphine ligand-; 5Y743P380H; MFCD01862440; BP-10059; 2-(di-tert-butylphos-phino)biphenyl; DTXSID50370169; di-tert-butylphosphino-biphenyl. CAS No. 224311-51-7. Molecular formula: C20H27P. Mole weight: 298.41g/mol. IUPAC Name: ditert-butyl-(2-phenylphenyl)phosphane. Rotatable Bond Count: 4. Exact Mass: 298.185g/mol. SMILES: CC (C) (C)P (C1=CC=CC=C1C2=CC=CC=C2)C (C) (C)C. InChI: InChI=1S/C20H27P/c1-19(2,3)21(20(4,5)6)18-15-11-10-14-17(18)16-12-8-7-9-13-16/h7-15H,1-6H3. InChIKey: CNXMDTWQWLGCPE-UHFFFAOYSA-N. Monoisotopic Mass: 298.185g/mol. | |
(2-Methylallyl)palladium(II) chloride dimer Quick inquiry Where to buy Suppliers range | yellow powder. Uses: Catalyst for: &bull Asymmetric allylic alkylation reactions &bull Suzuki-Miyaura reactions &bull Reductive cleavage reactions &bull Reaction of alkenyloxiranes with carbon monoxide. Group: Palladium series catalysts. Alternative Names: Chloro(2-methylallyl)palladium(II) dimer. Grades: 0.99. CAS No. 12081-18-4. Molecular formula: [CH2=C(CH3)CH2PdCl]2. Mole weight: 393.94. IUPAC Name: dichloropalladium; 2-methanidylprop-1-ene; palladium(2+). Exact Mass: 501.96400. Symbol: GHS07. Melting Point: 168.2-174.0ºC. InChIKey: CZAHDNZKZMLMCE-UHFFFAOYSA-L. H-Bond Donor: 0. H-Bond Acceptor: 4. Safty Description: 26. Hazard statements: Xi: Irritant. | |
(2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer, min. 98% Quick inquiry Where to buy Suppliers range | (2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer, min. 98%. Uses: Dimeric palladium precursor, that when treated with phosphines at room temperature in dichloromethane, provides Nsubstituted precatalysts. These catalysts are useful in the aminocarbonylation of (hetero)aryl bromides, and general C-C and C-N cross-coupling reactions. Alternative Names: MFCD29037176;(2'-Methylamino-1,1'-biphenyl-2-yl)methanesulfonatopalladium(II) dimer;1581285-85-9. CAS No. 1581285-85-9. Molecular formula: C28H30N2O6Pd2S2. Mole weight: 767.516g/mol. IUPAC Name: methanesulfonic acid;methyl-(2-phenylphenyl)azanide;palladium(2+). Exact Mass: 767.962g/mol. SMILES: C[N-]C1=CC=CC=C1C2=CC=CC=[C-]2. C[N-]C1=CC=CC=C1C2=CC=CC=[C-]2. CS(=O)(=O)O. CS(=O)(=O)O. [Pd+2]. [Pd+2]. InChI: InChI=1S/2C13H11N.2CH4O3S.2Pd/c2*1-14-13-10-6-5-9-12(13)11-7-3-2-4-8-11;2*1-5(2,3)4;;/h2*2-7,9-10H,1H3;2*1H3,(H,2,3,4);;/q2*-2;;;2*+2. InChIKey: RZJHFGLGMQFRAN-UHFFFAOYSA-N. H-Bond Donor: 2. H-Bond Acceptor: 10. Monoisotopic Mass: 765.961g/mol. | |
2- (Trifluoromethyl) phenyl trifluoromethane sulfonate Quick inquiry Where to buy Suppliers range | 2- (Trifluoromethyl) phenyl trifluoromethane sulfonate is used in the green synthetic preparation of N-aryl sulfonamides under mild reaction conditions with palladium nanoparticles as reusable catalysts. Group: Biochemicals. Grades: Highly Purified. CAS No. 199188-29-9. Pack Sizes: 250mg, 1g. Molecular Formula: C8H4F6O3S, Molecular Weight: 294.17. US Biological Life Sciences. | Worldwide |
4MetBuXPhos Pd G3 Quick inquiry Where to buy Suppliers range | 4MetBuXPhos Pd G3. Uses: Catalyst for cross-coupling reactions. Alternative Names: MFCD29037181;Me4 t-ButylXPhos Palladacycle Gen. 3;1507403-85-1;Methanesulfonato(2-di-t-butylphosphino-3,4,5,6-tetramethyl-2',4',6'-tri-i-propylbiphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II). CAS No. 1507403-85-1. Molecular formula: C46H67NO3PPdS+. Mole weight: 851.5g/mol. IUPAC Name: ditert-butyl-[2, 3, 4, 5-tetramethyl-6-[2, 4, 6-tri(propan-2-yl)phenyl]phenyl]phosphanium; methanesulfonic acid;palladium(2+);(2-phenylphenyl)azanide. Rotatable Bond Count: 7. Exact Mass: 850.361g/mol. SMILES: CC1=C (C (=C (C (=C1C)C2=C (C=C (C=C2C (C)C)C (C)C)C (C)C)[PH+] (C (C) (C)C)C (C) (C)C)C)C. CS (=O) (=O)O. C1=CC=C ([C-]=C1)C2=CC=CC=C2[NH-]. [Pd+2]. InChI: InChI=1S/C33H53P.C12H9N.CH4O3S.Pd/c1-19(2)26-17-27(20(3)4)30(28(18-26)21(5)6)29-24(9)22(7)23(8)25(10)31(29)34(32(11, 12)13)33(14, 15)16;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2, 3)4;/h17-21H, 1-16H3;1-6, 8-9, 13H;1H3, (H, 2, 3, 4);/q;-2;;+2/p+1. InChIKey: JMEGCNBORPOUMP-UHFFFAOYSA-O. H-Bond Donor: 2. H-Bond Acceptor: 5. Monoisotopic Mass: 850.361g/mol. | |
4- (Vinyloxymethyl) cyclohexanemethanol Quick inquiry Where to buy Suppliers range | 4- (Vinyloxymethyl) cyclohexanemethanol is used as a reagent in the synthesis of acetic acid esters by catalytic oxidation of vinyl ethers with aqueous H2O2 solutions in the presence of palladium catalysts having phosphine ligands and amines. Also used in the synthesis of Si-containing monomers and 4-substituted cyclohexane carbaldehydes. Group: Biochemicals. Grades: Highly Purified. CAS No. 114651-37-5. Pack Sizes: 1g, 10g. Molecular Formula: C10H18O2, Molecular Weight: 170.25. US Biological Life Sciences. | Worldwide |
5% Palladium on charcoal, 50% water Quick inquiry Where to buy Suppliers range | 1g Pack Size. Group: Building Blocks, Catalysts, Inorganic Chemicals. Formula: Pd. CAS No. 7440-5-3. Prepack ID 90022211-1g. Molecular Weight 106.42. See USA prepack pricing. | |
Allyl[1, 3-bis (2, 6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium (II) Quick inquiry Where to buy Suppliers range | Allyl[1, 3-bis (2, 6-diisopropylphenyl)-2-imidazolidinylidene]chloropalladium (II). Uses: Catalyst for the cross-coupling of aryl chlorides or bromides with aromatic amines. Catalyst for the α-arylation of ketones. Catalyst for anaerobic alcohol oxidation. Group: Heterocyclic Organic Compound. Alternative Names: ALLYLCHLORO[1,3-BIS(2,6-DI-I-PROPYLPHENYL)-4,5-DIHYDROIMIDAZOL-2-YLIDENE]PALLADIUM (II);Allylchloro[1, 3-bis(2, 6-di-i-propylphenyl)-4, 5-dihydroimidazol-2-ylidene]palladium(II), 97%;ALLYLCHLORO[1, 3-BIS-(DIISOPROPYLPHENYL)-2-IMIDAZOLIDINYLIDENE]PALLADIUM(II). Grades: 96%. CAS No. 478980-01-7. Molecular formula: C30H43ClN2Pd. Mole weight: 573.55. IUPAC Name: Allylchloro[1,3-bis(2,6-di-i-propylphenyl)-4,5-dihydroimidazol-2-ylide. Exact Mass: 572.21500. Safty Description: 26-36/37/39. | |
Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II) Quick inquiry Where to buy Suppliers range | white solid. Uses: Catalyst for the cross-coupling of aryl chlorides with boronic acids. Catalyst for the diamination of conjugated dienes and trienes. Catalyst for the dehalogenation of aryl chlorides. Catalyst for anaerobic alcohol oxidation. Catalyst for anaerobic ketone oxidation and domino oxidation/α-arylation. Group: Organic Phosphine Compounds. Alternative Names: Palladium, [1,?3-bis[2,?6-bis(1-methylethyl)?phenyl]?-1,?3-dihydro-2H-imidazol-2-ylidene]?chloro(η3-2-propen-1-yl)?-. Grades: 98%, Pd>18.5%. CAS No. 478980-03-9. Molecular formula: C30H42ClN2Pd. Mole weight: 572.54. Symbol: GHS07. Melting Point: > 300 °C (> 572 °F). Hazard statements: H315-H319-H335. | |
Allylchloro[1,3-bis-(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium(II) Quick inquiry Where to buy Suppliers range | Allylchloro[1,3-bis-(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium(II). Uses: Amination?Buchwald-Hartwig Aminaton; Cross Coupling Reactions with Arenes?Alpha Arylation; Cross Coupling Reactions with Arenes?Dehalogenation; Cross Coupling Reactions with Arenes?Kumada Coupling Reaction; Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Cross Coupling Reactions with Arenes?Oxidation; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction. Group: Catalysts for Pharmaceutical. CAS No. 478980-04-0. Molecular Weight: 487.38. Molecular Formula: C24H29N2ClPd. Purity: Metal purity 99.95. | |
Allylchloro[1,3-bis-(2,6-diisopropylphenyl)imidazol-2-idinylidene]palladium(II) Quick inquiry Where to buy Suppliers range | Allylchloro[1,3-bis-(2,6-diisopropylphenyl)imidazol-2-idinylidene]palladium(II). Uses: Amination?Buchwald-Hartwig Aminaton; Cross Coupling Reactions with Arenes?Alpha Arylation; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction. Group: Catalysts for Pharmaceutical. CAS No. 478980-01-7. Molecular Weight: 573.56. Molecular Formula: C30H43N2ClPd. Purity: Metal purity 99.95. | |
Allylchloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]palladium(II) Quick inquiry Where to buy Suppliers range | Allylchloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]palladium(II). Uses: Amination?Buchwald-Hartwig Aminaton; Cross Coupling Reactions with Arenes?Alpha Arylation; Cross Coupling Reactions with Arenes?Dehalogenation; Cross Coupling Reactions with Arenes?Kumada Coupling Reaction; Cross Coupling Reactions with Arenes?Mizoroki Heck Coupling Reaction; Cross Coupling Reactions with Arenes?Oxidation; Cross Coupling Reactions with Arenes?Suzuki-Miyaura Coupling Reaction; Dehalogenation; Oxidation; Telomerization. Group: Catalysts for Pharmaceutical; Oxidation. CAS No. 478980-03-9. Molecular Weight: 571.54. Molecular Formula: C30H41N2ClPd. Purity: Metal purity 99.95. | |
Allyldiphenylphosphine Quick inquiry Where to buy Suppliers range | Allyldiphenylphosphine. Uses: Cocatalyst in palladium catalyzed hydrocarboxylation reactions. Cocatalyst in Palladium catalyzed cross-coupling reactions. Ligand for hydroformylation catalysts. Ligand for the rhenium phosphinoborane pendant Lewis acid-assisted reductive coupling reactions. Catalyst precursor for alkene hydroboration. Group: Organic Phosphine Compounds. Alternative Names: Allyldiphenylphosphine; TRA0085191; allyl(diphenyl)phosphane; MFCD00014954; ST24045935; diphenyl(prop-2-enyl)phosphane; DB-009567; NSC-616248; DTXSID70181835; diphenyl(prop-2-enyl)phosphine. CAS No. 2741-38-0. Molecular formula: C15H15P. Mole weight: 226.259g/mol. IUPAC Name: diphenyl(prop-2-enyl)phosphane. Rotatable Bond Count: 4. Exact Mass: 226.091g/mol. SMILES: C=CCP(C1=CC=CC=C1)C2=CC=CC=C2. InChI: InChI=1S/C15H15P/c1-2-13-16(14-9-5-3-6-10-14)15-11-7-4-8-12-15/h2-12H,1,13H2. InChIKey: PDDYFPPQDKRJTK-UHFFFAOYSA-N. Monoisotopic Mass: 226.091g/mol. | |
Allylpalladium chloride dimer, Pd : 56.5 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: Application: Oxidant; Oxidation of Δ1-ene to enol acetate; Acetoxylation of aromatic hydrocarbons; Suzuki reaction, cross-coupling reaction, olefin carbonylation reaction. Group: Colloidal Catalysts. CAS No. 12012-95-2. Molecular Weight: 365.89 g/mol. SMILES: Cl[Pd]CC=C.Cl[Pd]CC=C. InChI: TWKVUTXHANJYGH-UHFFFAOYSA-L. Boiling Point: 216.3-223.7 ?. Flash Point: 98 %. | |
Allylpalladium chloride dimer, Pd : 58.2 % Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: Application: Oxidant; Oxidation of Δ1-ene to enol acetate; Acetoxylation of aromatic hydrocarbons; Suzuki reaction, cross-coupling reaction, olefin carbonylation reaction. Group: Colloidal Catalysts. CAS No. 12012-95-2. Molecular Weight: 365.89 g/mol. SMILES: Cl[Pd]CC=C.Cl[Pd]CC=C. InChI: TWKVUTXHANJYGH-UHFFFAOYSA-L. Boiling Point: 216.3-223.7 ?. Flash Point: 98 %. | |
Allylpalladium chloride dimer, supported on poly(ethylene glycol)polystyrene graft copolymer beads [~6% (C3H5PdCl)2] Quick inquiry Where to buy Suppliers range | Allylpalladium chloride dimer, supported on poly(ethylene glycol)polystyrene graft copolymer beads [~6% (C3H5PdCl)2]. Group: Palladium Catalysts. Molecular Formula: C6H10Cl2Pd2. | |
Allylpalladium(II) chloride dimer Quick inquiry Where to buy Suppliers range | Allylpalladium(II) chloride dimer. Uses: Precatalyst for the enantioselective hydrosilylation of olefins. Precatalyst for asymmetric allylic alkylation and amination. Used as a palladium source for cross-coupling reactions. Can be used with Trost ligands. Catalyst for the carbostannylation of alkynes. Used as a precatalyst for "-arylation of aldehydes. Group: Palladium series catalysts. Alternative Names: Di-mu-chlorodi-pi-allyldipalladium; NSC 151255; Bis(pi-allylpalladium chloride) (VAN); MFCD00044874 (95%); Bis(mu-chloro)bis(eta3-2-propenyl)dipalladium; AK327212; 12012-95-2; Palladium, di-pi-allyldi-mu-chlorodi- (8CI); Bis((eta3-allyl)(chloro)palladium); SC10406. CAS No. 12012-95-2. Molecular formula: C6H10Cl2Pd2. Mole weight: 365.886g/mol. IUPAC Name: chloropalladium(1+);prop-1-ene. Exact Mass: 365.823g/mol. EC Number: 234-579-8. SMILES: [CH2-]C=C.[CH2-]C=C.Cl[Pd+].Cl[Pd+]. InChI: InChI=1S/2C3H5.2ClH.2Pd/c2*1-3-2;;;;/h2*3H,1-2H2;2*1H;;/q2*-1;;;2*+2/p-2. InChIKey: PENAXHPKEVTBLF-UHFFFAOYSA-L. H-Bond Acceptor: 2. Monoisotopic Mass: 363.823g/mol. | |
Ammonium chloroiridate, Ir : 43 wt.% Quick inquiry Where to buy Suppliers range | Our company can provide customers with rich supported precious metal catalyst products such as palladium series, platinum series, rhodium series and ruthenium series. Our catalysts not only have high catalytic efficiency, strong selectivity, and recyclability, but also can be used in organic reactions such as hydrogenation, dehydrogenation, amination, and cyclization. In addition, some products can also be used as raw materials for various precious metal compounds. The company has formed a series of proprietary and characteristic process technologies, and is currently undergoing process improvement and upgrading. In short, our catalytic products can be widely used in medicine, new chemical materials, pesticides, dyes and pigments, environmental protection, new energy, electronics, basic chemicals and other fields. Uses: ·Used as a raw material for the preparation of iridium compounds such as iridium tetrachloride. Group: Colloidal Catalysts. CAS No. 16940-92-4. Molecular Weight: 441.01 g/mol. SMILES: [H][N+]([H])([H])[H]. [H][N+]([H])([H])[H]. Cl[Ir--](Cl)(Cl)(Cl)(Cl)Cl. InChI: LWNOUTCTZQNGEN-UHFFFAOYSA-J. Flash Point: 99 %. Purity: 2.86 g/mL at 25 °C (lit.). | |
Benzo[c][1,2,5]thiadiazol-5-ylboronic acid pinacol ester Quick inquiry Where to buy Suppliers range | Benzo[c][1,2,5]thiadiazol-5-ylboronic acid pinacol ester. Uses: Benzo[c][1,2,5]thiadiazol-5-ylboronic acid pinacol ester can be used as a reactant: To synthesize 5-methylbenzo[c][1,2,5]thiadiazole by methylation reaction with methyl iodide using palladium catalyst. In the Miyaura borylation and Suzuki coupling reactions. To prepare benzothiadiazole derivatives as potent PFKFB3 kinase inhibitors. Group: Dielectric Materials. CAS No. 1168135-03-2. IUPAC Name: 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole. Molecular Weight: C12H15BN2O2S. Molecular Formula: 262.14. SMILES: CC1(C)OB(OC1(C)C)c2ccc3nsnc3c2. | |
(Bicyclo[2.2.1]hepta-2,5-diene)dichloropalladium(II) Quick inquiry Where to buy Suppliers range | (Bicyclo[2.2.1]hepta-2,5-diene)dichloropalladium(II). Uses: Dichloro(norbornadiene)palladium(II) can be useful starting material for the in situ preparation of a variety of chiral and achiral palladium catalysts. Group: Palladium series catalysts. Alternative Names: TR-003664; (Bicyclo[2.2.1]hepta-2,5-diene)dichloropalladium(II), 98%; 2,5-Norbornadiene Palladium(II) Dichloride; SCHEMBL530639; CTK8A9533; NSC 176915; SC10472; AKOS015833821. CAS No. 12317-46-3. Molecular formula: C7H8Cl2Pd. Mole weight: 269.461g/mol. IUPAC Name: bicyclo[2.2.1]hepta-2,5-diene;dichloropalladium. Exact Mass: 267.904g/mol. EC Number: 235-583-2. SMILES: C1C2C=CC1C=C2.Cl[Pd]Cl. InChI: InChI=1S/C7H8.2ClH.Pd/c1-2-7-4-3-6(1)5-7;;;/h1-4,6-7H,5H2;2*1H;/q;;;+2/p-2. InChIKey: BNCRZJHZZCMDNP-UHFFFAOYSA-L. Monoisotopic Mass: 267.904g/mol. | |
Bis[1, 2-bis (diphenylphosphino)ethane]palladium (0) Quick inquiry Where to buy Suppliers range | Bis[1, 2-bis (diphenylphosphino)ethane]palladium (0). Uses: suzuki reaction. Group: Palladium series catalysts. Alternative Names: 31277-98-2; Pd(dppe)2; 2-diphenylphosphanylethyl (diphenyl)phosphane; BIS[1,2-BIS(DIPHENYLPHOSPHINO)ETHANE]-PALLADIUM; Pd(DIPHOS)2; bis(1,2-bis(diphenylphosphino)ethane)-palladium(0); RL03097; SCHEMBL541082; MFCD00009880; 3340AB. CAS No. 31277-98-2. Molecular formula: C52H48P4Pd. Mole weight: 903.271g/mol. IUPAC Name: 2-diphenylphosphanylethyl (diphenyl)phosphane; palladium. Rotatable Bond Count: 14. Exact Mass: 902.174g/mol. SMILES: C1=CC=C (C=C1) P (CCP (C2=CC=CC=C2) C3=CC=CC=C3) C4=CC=CC=C4. C1=CC=C (C=C1) P (CCP (C2=CC=CC=C2) C3=CC=CC=C3) C4=CC=CC=C4. [Pd]. InChI: InChI=1S/2C26H24P2.Pd/c2*1-5-13-23(14-6-1)27(24-15-7-2-8-16-24)21-22-28(25-17-9-3-10-18-25)26-19-11-4-12-20-26;/h2*1-20H,21-22H2; InChIKey: FAFGMAGIYHHRKN-UHFFFAOYSA-N. Monoisotopic Mass: 902.174g/mol. | |
Bis (3, 5, 3?, 5?-dimethoxydibenzylideneacetone) palladium (0) Quick inquiry Where to buy Suppliers range | Bis (3, 5, 3?, 5?-dimethoxydibenzylideneacetone) palladium (0). Uses: suzuki reaction. Group: Palladium series catalysts. Alternative Names: bis(3 5 3' 5'-dimethoxydibenzylideneace&; Bis(3,5,3',5 -dimethoxydibenzylideneacetone) palladium (0) ; bis (3, 5, 3', 5'-dimethoxydibenzylideneacetone) palladium; BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE; bis (3, 5, 3', 5'-dimethoxydibenzylideneacetone) palladium (0) , pd 13%; 811862-77-8; SC-90668; Bis(3,5,3',5 inverted exclamation marka-dimethoxydibenzylideneacetone) palladium (0) ; Bis (3, 5, 3', 5'-dimethoxydibenzylideneacetone) palladium (0) ; DTXSID10584705. CAS No. 811862-77-8. Molecular formula: C42H44O10Pd. Mole weight: 815.224g/mol. IUPAC Name: (1E,4E)-1,5-bis(3,5-dimethoxyphenyl)penta-1,4-dien-3-one;palladium. Rotatable Bond Count: 16. Exact Mass: 814.197g/mol. SMILES: COC1=CC (=CC (=C1)C=CC (=O)C=CC2=CC (=CC (=C2)OC)OC)OC. COC1=CC (=CC (=C1)C=CC (=O)C=CC2=CC (=CC (=C2)OC)OC)OC. [Pd]. InChI: InChI=1S/2C21H22O5.Pd/c2*1-23-18-9-15(10-19(13-18)24-2)5-7-17(22)8-6-16-11-20(25-3)14-21(12-16)26-4;/h2*5-14H,1-4H3;/b2*7-5+,8-6+; InChIKey: RTGAJOPJZJDWAX-XVGSOSPHSA-N. H-Bond Acceptor: 10. Monoisotopic Mass: 814.197g/mol. | |
Bis(acetonitrile)palladium(II) Dichloride Quick inquiry Where to buy Suppliers range | orange powder. Uses: Catalyst for the cyclization of δ-acetylenic carboxylic acids to butenolides. Catalyst for the aza-Michael reaction of carbamates with enones. Catalyst for the rearrangement of allylic imidates to allylic amides. Catalyst for the Nazarov cyclization of α-alkoxy dienones. Catalyst for the diamination of conjugated dienes. Three component Michael addition, cyclization, cross-coupling reaction. C-H activation of indoles. Catalyst used for the direct C-H arylation of isoxazoles at the 5 position. Group: Palladium series catalysts. Alternative Names: Palladium(II) chloride diacetonitrile complex. Grades: 99%,Pd >41. CAS No. 14592-56-4. Molecular formula: C4H6Cl2N2Pd. Mole weight: 259.43. IUPAC Name: acetonitrile; palladium(2+); dichloride. Exact Mass: 257.89400. Symbol: GHS06. Boiling Point: 63.5ºC at 760 mmHg. Flash Point: 5.6ºC. SMILES: CC#N.CC#N.[Cl-].[Cl-].[Pd+2]. InChIKey: RBYGDVHOECIAFC-UHFFFAOYSA-L. Safty Description: Danger. Hazard statements: H301-H311-H331. |