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| Product | Description | |
|---|---|---|
| 1,1'-Bis(di-isopropylphosphino)ferrocene palladium dichloride | 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). CAS No. 215788-65-1. Molecular formula: C22H36Cl2FeP2Pd. Mole weight: 595.64. Appearance: red crystalline powder. Purity: Pd >17.5%. IUPACName: cyclopentyl-di(propan-2-yl)phosphane;dichloropalladium;iron. Canonical 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]. Catalog: ACM215788651. |  |
| [1, 1'-Bis (diphenylphosphino) ferrocene]palladium (II) Dichloride Dichloromethane Adduct | [1, 1'-Bis (diphenylphosphino) ferrocene]palladium (II) Dichloride Dichloromethane Adduct. 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: Salt. Alternative Names: Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) Dichloromethane Adduct. CAS No. 95464-05-4. Product ID: [1, 1-Bis (diphenylphosphino) ferrocene]dichloropalladium (II) , complex wi. Molecular formula: 816.64. Mole weight: C34H28Cl2FeP2Pd·CH2Cl2. Pd ≥13.0%. |  |
| [1, 1'-Bis (diphenylphosphino) ferrocene]palladium (II) Dichloride Dichloromethane Adduct | 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. CAS No. 95464-05-4. Molecular formula: C34H28Cl2FeP2Pd·CH2Cl2. Mole weight: 816.64. Appearance: orange-red crystals. Purity: Pd ≥13.0%. IUPACName: [1, 1-Bis (diphenylphosphino) ferrocene]dichloropalladium (II) , complex wi. Density: 1 g/cm³. Catalog: ACM95464054. | |
| 1,1'-Bis (diphenylphosphino)ferrocene-palladium (II)dichloride dichloromethane complex | 1,1'-Bis (diphenylphosphino)ferrocene-palladium (II)dichloride dichloromethane complex. Uses: For analytical and research use. Group: Impurity standards. CAS No. 95464-05-4. Molecular Formula: C35H24Cl4FeP2Pd. Mole Weight: 810.59. Catalog: APB95464054. |  |
| [1, 1'-Bis (di-tert-butylphosphino) ferrocene]palladium (II) Dichloride | [1, 1'-Bis (di-tert-butylphosphino) ferrocene]palladium (II) Dichloride. Group: Biochemicals. Alternative Names: [1, 1'-Bis (di-tert-butylphosphino) ferrocene] dichloropalladium (II) ; Dichloro[1, 1'-bis (di-tert-butylphosphino) ferrocene]palladium (II) . Grades: Highly Purified. CAS No. 95408-45-0. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. US Biological Life Sciences. |  Worldwide |
| [1, 1'-Bis (di-tert-butylphosphino)ferrocene]palladium (II) Dichloride | 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). CAS No. 95408-45-0. Molecular formula: C26H44Cl2FeP2Pd. Mole weight: 651.75. Appearance: dark red crystals. Purity: Pd ≥16.3%. IUPACName: Dichloro[1, 1-Bis (di-Tert-Butylphosphino)Ferrocene]Palladium (II). Catalog: ACM95408450. | |
| [1, 4-Bis (diphenylphosphino) butane]palladium (II) Dichloride | [1, 4-Bis (diphenylphosphino) butane]palladium (II) Dichloride. Group: Biochemicals. Alternative Names: Dichloro[1, 4-bis (diphenylphosphino) butane]palladium (II) . Grades: Highly Purified. CAS No. 29964-62-3. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Bis(acetonitrile)palladium(II) dichloride | Bis(acetonitrile)palladium(II) dichloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 14592-56-4. Pack Sizes: 250 mg; 500 mg. Product ID: HY-W002087. |  |
| Bis(acetonitrile)palladium(II) Dichloride | Bis(acetonitrile)palladium(II) Dichloride. 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: Salt. Alternative Names: Palladium(II) chloride diacetonitrile complex. CAS No. 14592-56-4. Product ID: acetonitrile; palladium(2+); dichloride. Molecular formula: 259.43. Mole weight: C4H6Cl2N2Pd. CC#N.CC#N.[Cl-].[Cl-].[Pd+2]. RBYGDVHOECIAFC-UHFFFAOYSA-L. 99%,Pd >41. | |
| Bis(acetonitrile)palladium(II) Dichloride | 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. CAS No. 14592-56-4. Molecular formula: C4H6Cl2N2Pd. Mole weight: 259.43. Appearance: orange powder. Purity: 99%,Pd >41. IUPACName: acetonitrile; palladium(2+); dichloride. Canonical SMILES: CC#N.CC#N.[Cl-].[Cl-].[Pd+2]. Catalog: ACM14592564. | |
| Bis(benzonitrile)palladium(II) Dichloride | 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. Group: Palladium series catalysts. Alternative Names: ST24046185; bis(benzonitrile)-palladium(II) chloride; J-007619; bis(chloranyl)palladium; MFCD00013123 (95+%); SCHEMBL63930; Bis(phenylnitrile)dichloropalladium; NSC635160; PdCl2(PhCN)2; bis(benzonitrile)dichloro-palladium (II). CAS No. 14220-64-5. Molecular formula: C14H10Cl2N2Pd. Mole weight: 383.568g/mol. IUPACName: benzonitrile;dichloropalladium. Canonical SMILES: C1=CC=C(C=C1)C#N. C1=CC=C(C=C1)C#N. Cl[Pd]Cl. ECNumber: 238-085-3. Catalog: ACM14220645. | |
| Bis ( methyl diphenylphosphine) palladium (II) Dichloride | Bis ( methyl diphenylphosphine) palladium (II) Dichloride. Group: Biochemicals. Alternative Names: Dichlorobis ( methyl diphenylphosphine) palladium (II) . Grades: Highly Purified. CAS No. 52611-08-2. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Bis (tri cyclohexylphosphine) palladium (II) Dichloride | Bis (tri cyclohexylphosphine) palladium (II) Dichloride. Group: Biochemicals. Alternative Names: Dichlorobis (tri cyclohexylphosphine) palladium (II) . Grades: Highly Purified. CAS No. 29934-17-6. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Bis (tricyclohexylphosphine)palladium (II) Dichloride | suzuki reaction. Group: Palladium series catalysts. Alternative Names: Dichlorobis (tricyclohexylphosphine)palladium (II), 95%; KS-00000W5G; AC-5515; MFCD00191830; RW2241; 29934-17-6; AKOS015917339; 934D176; TRANS-DICHLOROBIS (TRICYCLOHEXYLPHOSPHINE)PALLADIUM (II); I14-9522. CAS No. 29934-17-6. Molecular formula: C36H66Cl2P2Pd. Mole weight: 738.192g/mol. IUPACName: dichloropalladium; tricyclohexylphosphane. Canonical SMILES: C1CCC(CC1)P(C2CCCCC2)C3CCCCC3. C1CCC(CC1)P(C2CCCCC2)C3CCCCC3. Cl[Pd]Cl. Catalog: ACM29934176. | |
| Bis (tri-o-tolylphosphine) palladium (II) Dichloride | Bis (tri-o-tolylphosphine) palladium (II) Dichloride. Group: Biochemicals. Alternative Names: Dichlorobis (tri-o-tolylphosphine) palladium (II) . Grades: Highly Purified. CAS No. 40691-33-6. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Bis(tri-o-tolylphosphine)palladium(II) Dichloride | Coupling reaction of aryl bromides with vinylic acetates. Group: Palladium series catalysts. Alternative Names: 5531AB; SC10409; MFCD00274659 (98%); dichlorobis(tri-o-tolyl-phosphine)palladium(II); dichlorobis(tri-O-tolylphosphine)-palladium (II); DICHLOROBIS(TRI-ORTHO-TOLYLPHOSPHINE)PALLADIUM(II); FT-0696077; bis[tri(ortho-tolyl)phosphine] palladium chloride; Dichlorobis(tri-o-tolylphosphine)palladium; AK-76768. CAS No. 40691-33-6. Molecular formula: C42H42Cl2P2Pd. Mole weight: 786.066g/mol. IUPACName: dichloropalladium;tris(2-methylphenyl)phosphane. Canonical SMILES: CC1=CC=CC=C1P (C2=CC=CC=C2C)C3=CC=CC=C3C. CC1=CC=CC=C1P (C2=CC=CC=C2C)C3=CC=CC=C3C. Cl[Pd]Cl. Catalog: ACM40691336. | |
| Bis (triphenylphosphine) palladium (II) dichloride | Bis (triphenylphosphine) palladium (II) dichloride. Group: Biochemicals. Alternative Names: Dichlorobis (triphenylphosphine) palladium (II) . Grades: Highly Purified. CAS No. 13965-03-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C36H30Cl2P2Pd. US Biological Life Sciences. | Worldwide |
| Bis(triphenylphosphine)palladium(II) Dichloride | Bis(triphenylphosphine)palladium(II) Dichloride. Uses: Precatalyst for the carbonylative cyclization of malonate derivatives. catalyst used in the double allylation of activated olefins. precatalyst for the three-component preparation of 3-arylidene- (or 3-alkenylidene) tetrahydrofurans. precatalyst for the homocoupling of terminal alkynes. precatalyst in the cross-coupling of alkynylsilanols and aryl halides. catalyst for direct pd-catalyzed alkynylation of n-fused heterocycles. catalyst for a tandem heck reaction/c-h functionalization. catalyst for direct arylation of tautomerizable heterocycles. Group: Salt. Alternative Names: TRANS-BIS-(TRIPHENYLPHOSPHINE)PALLADIUM DICHLORIDE; 13965-03-2; 28966-81-6; AC1L36TY; SC-01002; LS-192238; bis(triphenylphosphine) palladiuml(II) dichloride; bis(triphenylphosphine) palladium (II) chloride; FC0823; EINECS 237-744-2. CAS No. 13965-03-2. Product ID: palladium(2+); triphenylphosphane; dichloride. Molecular formula: 701.904g/mol. Mole weight: C36H30Cl2P2Pd. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Cl-]. [Cl-]. [Pd+2]. InChI=1S/2C18H15P. 2ClH. Pd/c2*1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18; ; ; /h2*1-15H; 2*1H; /q; ; ; ; +2/p-2. YNHIGQDRGKUECZ-UHFFFAOYSA-L. | |
| Bis(triphenylphosphine)palladium(II) Dichloride | Precatalyst for the carbonylative cyclization of malonate derivatives. Catalyst used in the double allylation of activated olefins. Precatalyst for the three-component preparation of 3-arylidene- (or 3-alkenylidene) tetrahydrofurans. Precatalyst for the homocoupling of terminal alkynes. Precatalyst in the cross-coupling of alkynylsilanols and aryl halides. Catalyst for direct Pd-catalyzed alkynylation of N-fused heterocycles. Catalyst for a tandem Heck reaction/C-H functionalization. Catalyst for direct arylation of tautomerizable heterocycles. Group: Palladium series catalysts. Alternative Names: TRANS-BIS-(TRIPHENYLPHOSPHINE)PALLADIUM DICHLORIDE; 13965-03-2; 28966-81-6; AC1L36TY; SC-01002; LS-192238; bis(triphenylphosphine) palladiuml(II) dichloride; bis(triphenylphosphine) palladium (II) chloride; FC0823; EINECS 237-744-2. CAS No. 13965-03-2. Molecular formula: C36H30Cl2P2Pd. Mole weight: 701.904g/mol. IUPACName: palladium(2+); triphenylphosphane; dichloride. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Cl-]. [Cl-]. [Pd+2]. ECNumber: 237-744-2. Catalog: ACM13965032. | |
| Bis (triphenylphosphine) palladiuml(II) dichloride 99+% (Palladium content:15 | Bis (triphenylphosphine) palladiuml(II) dichloride 99+% (Palladium content:15. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences. | Worldwide |
| Poly[N-isopropylacrylamide-co-4-(diphenylphosphino)styrene] Palladium(II) Dichloride (ratio, acrylamide:phosphine=20:2) | Poly[N-isopropylacrylamide-co-4-(diphenylphosphino)styrene] Palladium(II) Dichloride (ratio, acrylamide:phosphine=20:2). Group: Polystyrene (ps). | |
| [1, 1'-Bis (di-cyclohexylphosphino) ferrocene]dichloropalladium (II) | 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). CAS No. 917511-90-1. Molecular formula: C34H52Cl2FeP2Pd. Mole weight: 755.9. Appearance: red crystalline powder. Purity: Pd >14.0%. IUPACName: dichloropalladium; dicyclohexyl(cyclopentyl)phosphane; iron. Canonical 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]. Catalog: ACM917511901. | |
| (1, 1'-Bis (diphenylphosphino) ferrocene) dichloropalladium-dichloromethane | (1, 1'-Bis (diphenylphosphino) ferrocene) dichloropalladium-dichloromethane is used in the preparation of imidazoles, benzimidazoles, and tetrahydropyrimidines. Group: Biochemicals. Alternative Names: Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) dichloromethane adduct; [1, 1'-Bis (diphenylphosphino) ferrocene]palladium dichloride dichloromethane adduct; [1, 1'-Bis (diphenylphosphino) ferrocene]palladium dichloride methylene chloride adduct; [1, 1'-Bis (diphenylphosphino) ferrocene]palladium (II) chloride Dichloromethane Adduct; (SP-4-2) -[1, 1'-bis (diphenylphosphino) ferrocene-P, P']dichloropalladium Compd. with Dichloromethane; 1, 1'-bis (diphenylphosphino) ferrocene Palladium Complex. Grades: Highly Purified. CAS No. 95464-05-4. Pack Sizes: 1g, 2.5g. Molecular Formula: C??H??Cl?FeP?Pd. CH ?Cl?, Molecular Weight: 816.64. US Biological Life Sciences. | Worldwide |
| (1, 1'-Bis (diphenylphosphino) ferrocene) dichloropalladium Toluene | (1, 1'-Bis (diphenylphosphino) ferrocene) dichloropalladium Toluene is used in the preparation of imidazoles, benzimidazoles, and tetrahydropyrimidines. Group: Biochemicals. Alternative Names: Dichloro[1, 1'-bis (diphenylphosphino) ferrocene]palladium (II) Toluene Adduct; [1, 1'-Bis (diphenylphosphino) ferrocene]palladium DIchloride Toluene Adduct; [1, 1'-Bis (diphenylphosphino) ferrocene]palladium Dichloride Toluene Chloride Adduct; [1, 1'-Bis (diphenylphosphino) ferrocene]palladium (II) Chloride Toluene Adduct; (SP-4-2) -[1, 1'-bis (diphenylphosphino) ferrocene-P, P']dichloropalladium Compd. with Toluene; 1, 1'-bis (diphenylphosphino) ferrocene Palladium Complex. Grades: Highly Purified. CAS No. 867381-03-1. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| (1, 3-Bis (diphenylphosphino)propane)palladium (II) chloride | 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. IUPACName: dichloropalladium; 3-diphenylphosphanylpropyl (diphenyl)phosphane. Canonical SMILES: C1=CC=C (C=C1) P (CCCP (C2=CC=CC=C2) C3=CC=CC=C3) C4=CC=CC=C4. Cl[Pd]Cl. Catalog: ACM59831026. | |
| (Bicyclo[2.2.1]hepta-2,5-diene)dichloropalladium(II) | 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. IUPACName: bicyclo[2.2.1]hepta-2,5-diene;dichloropalladium. Canonical SMILES: C1C2C=CC1C=C2.Cl[Pd]Cl. ECNumber: 235-583-2. Catalog: ACM12317463. | |
| Crotylpalladium chloride dimer | Heterocyclic Organic Compound. Alternative Names: (2-Butenyl)chloropalladium dimer, Di-2-butenyldipalladium dichloride, Dichlorobis(1-methylallyl)dipalladium, 12081-22-0, Di-|Eth-Crotylpalladium chloride, CROTYLPALLADIUM CHLORIDE DIMER, DI-PI-CROTYLPALLADIUM CHLORIDE, SC10504, Bis[(1,2,3-|C)-2-buten-1-yl]di-|I-chlorodi-palladiumdi-|Eth-crotylpalladium chloride, BIS[(1,2,3-ETA)-2-BUTEN-1-YL]DI-MU-CHLORODI-PALLADIUMDI-PI-CROTYLPALLADIUM CHLORIDE. CAS No. 12081-22-0. Molecular formula: C8H14Cl2Pd2. Mole weight: 393.94. Purity: 0.96. IUPACName: (E)-but-2-ene;chloropalladium(1+). Canonical SMILES: CC=C[CH2-]. CC=C[CH2-]. Cl[Pd+]. Cl[Pd+]. Catalog: ACM12081220. | |
| Dichloro[9, 9-dimethyl-4, 5-bis (diphenylphosphino) xanthene]palladium (II) | Dichloro[9, 9-dimethyl-4, 5-bis (diphenylphosphino) xanthene]palladium (II) . Group: Biochemicals. Alternative Names: [4, 5-Bis (diphenylphosphino) -9, 9-dimethylxanthene] dichloropalladium (II) ; [4, 5-Bis (diphenylphosphino) -9, 9-dimethylxanthene] palladium (II) Dichloride. Grades: Highly Purified. CAS No. 205319-10-4. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences. | Worldwide |
| Dichloro{bis[2- (diphenylphosphino) phenyl]ether}palladium (II) , 98% | Stereoretentive palladium-catalyzed Kumada-Corriu couplings of alkenyl halides at room temperature. Highly selective reactions of unbiased alkenyl halides: Negishi-Plus couplings. Group: Heterocyclic organic compound. Alternative Names: DTXSID10463965; SCHEMBL2126742; AK308026; [2- (2-diphenylphosphanylphenoxy) phenyl]-diphenylphosphane; KS-00000ZP2; dichloropalladium; BIS(DIPHENYLPHOSPHINOPHENYL)ETHER PALLADIUM(II) DICHLORIDE; AKOS027320681; 205319-06-8. CAS No. 205319-06-8. Molecular formula: C36H28Cl2OP2Pd. Mole weight: 715.887g/mol. IUPACName: dichloropalladium; [2- (2-diphenylphosphanylphenoxy) phenyl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1) P (C2=CC=CC=C2) C3=CC=CC=C3OC4=CC=CC=C4P (C5=CC=CC=C5) C6=CC=CC=C6. Cl[Pd]Cl. Catalog: ACM205319068. | |
| Dichlorobis (triphenylphosphine) Palladium (II) | Dichlorobis (triphenylphosphine) Palladium (II) is used primarily in organometallic catalytic reactions due to the palladium content of the compound. It is also involved in crystalized structures of metallacyclic complexes which show antiinflammatory and antifungal properties. Group: Biochemicals. Alternative Names: Bis (triphenylphosphine) dichloropalladium; Bis (triphenylphosphine) palladium Chloride; Bis (triphenylphosphine) palladium Dichloride; Bis (triphenylphosphine) palladium (II) Chloride; Bis (triphenylphosphine) palladium (II) Dichloride; Bis (triphenylphosphino) palladium Chloride; Dichlorobis (triphenylphosphine) palladium; Dichlorobis (triphenylphosphine) palladium (II) ; NSC 122924; Palladiumbis (triphenylphosphine) Dichloride. Grades: Highly Purified. CAS No. 13965-03-2. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| Dichloro (N, N, N', N'-tetramethylethylenediamine) palladium (II) | Catalyst for: Cross-coupling reactions. Catalytic reduction reactions. Preparation of silyl ethers via reaction of silicon-hydrogen bond with alcohols. Oxidative carbonylation reactions. Group: Palladium series catalysts. Alternative Names: I14-10025; AC1L4Z7Y; AC1Q1RTB; Palladium, dichloro(N,N,N',N'-tetramethyl-1,2-ethanediamine-N,N')-, (SP-4-2)- (9CI); RL01764; Palladium, dichloro(N, N, N', N'-tetramethylethylenediamine)- (8CI); AKOS015900158; TRA0000186; dichloride. CAS No. 14267-08-4. Molecular formula: C6H16Cl2N2Pd. Mole weight: 293.528g/mol. IUPACName: palladium(2+);N, N, N', N'-tetramethylethane-1, 2-diamine;dichloride. Canonical SMILES: CN(C)CCN(C)C.[Cl-].[Cl-].[Pd+2]. Catalog: ACM14267084. | |
| Dichloro[(R)-(+)-2,2'-bis(di-2-furanylphosphino)-6,6'-dimethoxy-1,1'-biphenyl]palladium(II) | This Palladium-complex is used for the asymmetric cross-coupling of allylboron reagents with allylic electrophiles. The catalyst is used for the kinetic resolution of propargylic acetates to give enantioenriched 1,5-enynes. Group: Palladium catalysts. Alternative Names: [2-[2-[Bis(furan-2-yl)phosphanyl]-6-methoxyphenyl]-3-methoxyphenyl]-bis(furan-2-yl)phosphane; palladium(2+); dichloride. CAS No. 1338245-54-7. Molecular formula: C30H24Cl2O6P2Pd. Mole weight: 719.78. Appearance: Pale yellow powder. Purity: 0.98. Canonical SMILES: COC1=C (C (=CC=C1)P (C2=CC=CO2)C3=CC=CO3)C4=C (C=CC=C4P (C5=CC=CO5)C6=CC=CO6)OC. [Cl-]. [Cl-]. [Pd+2]. Catalog: ACM1338245547-1. | |
| Palladium(II) chloride | Palladium(II) chloride, also known as palladium dichloride and palladous chloride, are the chemical compounds with the formula PdCl2. PdCl2 is a common starting material in palladium chemistry - palladium-based catalysts are of particular value in organic synthesis. It is prepared by chlorination of palladium. Uses: C-h activation; carbonylation; cross coupling reactions with arenes→mizoroki heck coupling reaction; oxidation. Group: Electrolytes. Alternative Names: Palladium chloride (PdCl2); dichloropalladium; Palladium(II) Chloride. CAS No. 7647-10-1. Product ID: dichloropalladium. Molecular formula: 177.31. Mole weight: Cl2Pd. Cl[Pd]Cl. InChI=1S/2ClH.Pd/h2*1H;/q;;+2/p-2. PIBWKRNGBLPSSY-UHFFFAOYSA-L. Metal purity 99.95. | |
| Palladium(II) chloride | Palladium(II) chloride, also known as palladium dichloride and palladous chloride, are the chemical compounds with the formula PdCl2. PdCl2 is a common starting material in palladium chemistry - palladium-based catalysts are of particular value in organic synthesis. It is prepared by chlorination of palladium. Uses: C-h activation; carbonylation; cross coupling reactions with arenes→mizoroki heck coupling reaction; oxidation. Group: Metal & ceramic materials. Alternative Names: Palladium chloride (PdCl2); dichloropalladium; Palladium(II) Chloride. CAS No. 7647-10-1. Molecular formula: Cl2Pd. Mole weight: 177.31. Appearance: Dark brown powder. Purity: Metal purity 99.95. IUPACName: dichloropalladium. Canonical SMILES: Cl[Pd]Cl. Density: 4. ECNumber: 231-596-2. Catalog: ACM7647101-3. | |
| Palladium (II) Chloride | PALLADIUM (II) CHLORIDE, 99.9% pure, -8 mesh, (Synonym: Palladium Dichloride), Formula: PdCl2. CAS No. 1947-10-1. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Palladium(II)(π-cinnamyl) Chloride Dimer | Precursor for the preparation of a palladium catalyst used in the carbonylative arylation of ketones, yielding vinylbenzoate compounds. Precursor for the preparation of a palladium catalyst used in the Buchwald-Hartwig amination of (hetero)aryl chlorides. Precursor for the preparation of a palladium catalyst used in the arylative dearomatization of phenols. Versatile palladium precursor for the preparation of palladium catalysts used in the cross-coupling of aryl chlorides and amines , conversion of aryl triflates to aryl fluorides , and the α-arylation of aldehydes. Group: Palladium series catalysts. Alternative Names: 12131-44-1;Palladium(|Eth-cinnamyl) chloride dimer;AK136149;PALLADIUM(PI-CINNAMYL) CHLORIDE DIMER;Di- -chlorobis[(1,2,3- )-1-phenyl-2-propen-1-yl]dipalladium;Di-|I-chlorobis[(1,2,3-|C)-1-phenyl-2-propen-1-yl]dipalladium;Di-|I-chlorobis[(1,2,3-|C)-1-phenyl-2-propenyl]dipalladium(II);Di-mu-chlorobis[(1,2,3-eta)-1-phenyl-2-propen-1-yl]dipalladium. CAS No. 12131-44-1. Molecular formula: C18H18Cl2Pd2. Mole weight: 518.082g/mol. IUPACName: palladium(2+);prop-2-enylbenzene;dichloride. Canonical SMILES: C=C[CH-]C1=CC=CC=C1. C=C[CH-]C1=CC=CC=C1. [Cl-]. [Cl-]. [Pd+2]. [Pd+2]. Catalog: ACM12131441. | |
| Sensitizer | Sensitizer. Uses: Tetraamminepalladium(II) chloride monohydrate is used to prepare trans-diamminedichloropalladium(II). it is also utilized in the preparation of mesoporous carbon supporting palladium nanoparticles by using graphite oxide. it is used as catalysts, reagents, and analytical reagents. Group: Salt. Alternative Names: Tetraamminepalladium(II) chloride monohydrate; KS-00000H5G; AKOS027250697; chloride hydrate; MFCD00151033; Palladium(2+), tetraammine-, dichloride, monohydrate, (SP-4-1)- (9CI); TETRAAMMINEPALLADIUM (II) CHLORIDE; Sensitizer; ST24050111. CAS No. 13933-31-8. Product ID: azane; dichloropalladium; hydrate. Molecular formula: 263.459g/mol. Mole weight: Cl2H14N4OPd. N.N.N.N.O.Cl[Pd]Cl. InChI=1S/2ClH.4H3N.H2O.Pd/h2*1H; 4*1H3; 1H2; /q; ; ; ; ; ; ; +2/p-2. WVCXSPJPERKPJS-UHFFFAOYSA-L. | |
| Sensitizer | Tetraamminepalladium(II) chloride monohydrate is used to prepare trans-diamminedichloropalladium(II). It is also utilized in the preparation of mesoporous carbon supporting palladium nanoparticles by using graphite oxide. It is used as catalysts, reagents, and analytical reagents. Group: Metal & ceramic materials. Alternative Names: Tetraamminepalladium(II) chloride monohydrate; KS-00000H5G; AKOS027250697; chloride hydrate; MFCD00151033; Palladium(2+), tetraammine-, dichloride, monohydrate, (SP-4-1)- (9CI); TETRAAMMINEPALLADIUM (II) CHLORIDE; Sensitizer; ST24050111. CAS No. 13933-31-8. Molecular formula: Cl2H14N4OPd. Mole weight: 263.459g/mol. IUPACName: azane;dichloropalladium;hydrate. Canonical SMILES: N.N.N.N.O.Cl[Pd]Cl. Catalog: ACM13933318. | |
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