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| Product | Description | |
|---|---|---|
| Palladium Oxide Nanopowder | Palladium Oxide Nanopowder. Group: Oxides nanoparticles. CAS No. 1314-08-5. Molecular formula: 122.42 g/mol. Mole weight: PdO. 99.9%. |  |
| Palladium (II) Oxide | PALLADIUM (II) OXIDE, ANHYDROUS, 99.9% pure, -20 mesh, (Synonym: Palladium Monoxide), Formula: PdO. CAS No. 1314-08-5. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Palladium (II) Oxide, anhydrous | Palladium (II) Oxide, anhydrous. Grades: 99.9% Extremely High (>=99%). CAS No. 1314-08-5. Order Number: 2815. |  www.prochemonline.com |
| Palladium(II) oxide hydrate | Palladium(II) oxide hydrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: PALLADIUM OXIDE;PALLADIUM(+2)OXIDE;PALLADIUM(II) OXIDE HYDRATE;Palladium(II) oxide monohydrate;Palladium(II) oxide hydrate, 99.9+%;PALLADIUM (II) OXIDE, 99.9% (METALS BASIS), PD 75.3% MIN;Palladium(II) oxide monohydrate, 99.9% (metals basis), Pd 73% min;P. Product Category: Metal & Ceramic Materials. CAS No. 64109-12-2. Molecular formula: OPd. Mole weight: 122.42 (anhydrous basis). Product ID: ACM64109122. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Palladium monoxide | Palladium monoxide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CTK4B7267; AC1NO7R7; 1314-08-5; oxopalladium; Palladium(II) oxide, anhydrous; TR-004294; RTR-004294; Palladium oxide (PdO); HBEQXAKJSGXAIQ-UHFFFAOYSA-N; ACMC-1BQVH. Product Category: Nanoparticles & Nanopowders. CAS No. 1314-08-5. Molecular formula: OPd. Mole weight: 122.419g/mol. IUPACName: oxopalladium. Canonical SMILES: O=[Pd]. ECNumber: 215-218-3. Product ID: ACM1314085. Alfa Chemistry ISO 9001:2015 Certified. | |
| Reduced Graphene Oxide Powder, decorated with Palladium Nanoparticles | Reduced Graphene Oxide (RGO) Powder decorated with Palladium Nanoparticles is graphene-metal hybrid material composed of reduced graphene oxide (r-GO) and a broad distribution of nanoscale palladium particles. Applications include electron microscopy imaging and as a catalyst material in fuel cells. Uses: Electrocatalyst. field-effect transistors. sensors. lithium ion batteries. supercapacitors. Group: other nano materials. Alternative Names: RGO-Pd, reduced graphene oxide nanosheets decorated with Pd NPs. Mole weight: CxOzyHz. | |
| 1,1'-Bis(di-isopropylphosphino)ferrocene palladium dichloride | 1,1'-Bis(di-isopropylphosphino)ferrocene palladium dichloride. 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. Additional or Alternative Names: PdCl2(dippf). Product Category: Palladium series catalysts. Appearance: red crystalline powder. CAS No. 215788-65-1. Molecular formula: C22H36Cl2FeP2Pd. Mole weight: 595.64. 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]. Product ID: ACM215788651. Alfa Chemistry ISO 9001:2015 Certified. Categories: DTXSID70746347. | |
| 2-Mercaptopyridine N-Oxide Sodium Salt | 2-Mercaptopyridine N-oxide sodium salt is a bidentate complexing agent used to chelate transition metals at a pH range of 0.7-7.4. 2-Mercaptopyridine N-oxide sodium salt is also used as a selective absorptiometric reagent in the determination of palladium. Group: Biochemicals. Grades: Highly Purified. CAS No. 3811-73-2. Pack Sizes: 2.5g, 10g. Molecular Formula: C5H4NNaOS, Molecular Weight: 149.15. US Biological Life Sciences. |  Worldwide |
| [ (2Z) -2- [ (3S, 5R) -3, 5-Bis [ [ (1, 1-dimethylethyl) dimethylsilyl] oxy] -2-methylenecyclohexylidene] ethyl] diphenylphosphine Oxide | The biphenyl-P-oxide compound, widely applied in biomedicine such as drug discovery, serves as a palladium-catalyzed cross-coupling reaction ligand. This compound presents tremendous versatility in its usability as it is instrumental in the oligonucleotide synthesis and the production of numerous bioactive molecules. Synonyms: [3S- (1Z, 3α , 5β ) ] - [2- [3, 5-Bis [ [ (1, 1-dimethylethyl) dimethylsilyl] oxy] -2-methylenecyclohexylidene] ethyl] diphenylphosphine Oxide; Phosphine oxide, [2- [3, 5-bis [ [ (1, 1-dimethylethyl) dimethylsily] oxy] -2-methylenecyclohexylidene] ethyl] diphenyl-, [3S-(1Z,3α,5β)]-; Tert-butyl-[(1R,3S,5Z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane; ( (Z) -2- ( (3S, 5R) -3, 5-bis ( (tert-butyldimethylsilyl) oxy) -2-methylenecyclohexylidene) ethyl) diphenylphosphine oxide. Grades: 95%. CAS No. 81522-68-1. Molecular formula: C33H51O3PSi2. Mole weight: 582.90. |  |
| Palladium-coated Carbon Nanotubes | Palladium-coated Carbon Nanotubes. Group: Metal and metal oxide nanoparticles coated cnt. | |
| 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. | |
| Silver acetate | Silver acetate is an inorganic compound with the empirical formula CH3CO2Ag (or AgC2H3O2). It is a photosensitive, white, crystalline solid. It is a useful reagent in the laboratory as a source of silver ions lacking an oxidizing anion. It has been used in some antismoking drugs. Uses: 3 - 1 - carbonylation silver acetate, when combined with carbon monoxide (co), can induce the carbonylation of primary and secondary amines. other silver salts can be used but the acetate gives the best yield. 2 r2nh + 2 agoac + co → [r2n]2co + 2 hoac + 2 ag 3 - 2 - hydrogenation silver acetate in a solution of pyridine absorbs hydrogen and is reduced to metallic silver. 3 - 3 - direct ortho - arylation silver acetate is a useful reagent for direct ortho-arylation (to install two adjacent substituents on an aromatic ring) for of benzylamines and n-methylbenzylamines. the reaction is palladiumcatalized and requires a slight excess of silver acetate.this reaction is shorter than previous ortho-arylation methods. Group: Solution deposition precursors. Alternative Names: Acetic acid silver(I) salt. CAS No. 563-63-3. Product ID: Silver; acetate. Molecular formula: 166.91. Mole weight: C2H3AgO2. CC(=O)[O-].[Ag+]. InChI=1S/C2H4O2.Ag/c1-2(3)4;/h1H3, (H, 3, 4);/q;+1/p-1. CQLFBEKRDQMJLZ-UHFFFAOYSA-M. 95%+. | |
| (1S)-1-Amino-2-methyl-1-phenylpropan-2-ol | (1S)-1-Amino-2-methyl-1-phenylpropan-2-ol can be used as reactant/reagent in stereoselective preparation of diaryl carbonyl compounds via palladium-catalyzed enantioselective redox-relay oxidative Heck arylation of arylboronic acids and homoallylic alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 110480-86-9. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H15NO, Molecular Weight: 165.23. US Biological Life Sciences. | Worldwide |
| 2,2'-Bis(diphenylphosphino)biphenyl | 2,2'-Bis(diphenylphosphino)biphenyl. Uses: Supporting ligand in a chiral diamine-ruthenium system for the enantioselective hydrogenation of ketones. useful ligand for palladium-catalyzed amination and kumada cross-coupling reactions useful ligand for palladium-catalyzed synthesis of butatrenes. useful ligand for iridium-catalyzed c-c cross-coupling of allenes with primary alcohols via transfer hydrogenation. useful ligand for iridium-catalyzed c-c cross-coupling of dienes with primary alcohols via transfer hydrogenation. useful ligand for iridium-catalyzed c-c cross-coupling of allylic gem-dicarboxylates with aldehydes via transfer hydrogenation. useful ligand for the palladium-catalyzed synthesis of chiral allenylsilanes. ruthenium-catalyzed synthesis of indoles. ruthenium-catalyzed oxidative cyclization. rhodium-catalyzed boron arylation. Additional or Alternative Names: BIPHEP; MFCD03094574; AKOS015911364; DB-009479; 1,1'-[[1,1'-BIPHENYL]-2,2'-DIYL]BIS[1,1-DIPHENYL]-PHOSPHINE; CTK3J1519; SCHEMBL1120987; 2,2'-Bis(diphenylphosphino)biphenyl; 2,2'-bis(diphenylphosphanyl)-1,1'-biphenyl; FT-0657577. Product Category: Organic Phosphine Compounds. CAS No. 84783-64-2. Molecular formula: C36H28P2. Mole weight: 522.568g/mol. IUPACName: [2-(2-diphenylphosphanylphenyl)phenyl]-diphenylphosphane. Canonical SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3C4=CC=CC=C4P(C5=CC=CC=C5)C6=CC=CC=C6. Product ID: ACM84783642. | |
| 2-(Dicyclohexylphosphino)biphenyl | 2-(Dicyclohexylphosphino)biphenyl. Uses: Ligand used in the palladium-catalyzed synthesis of aromatic amines from aryl chlorides, bromides and triflates. ligand employed in suzuki coupling reactions involving aryl chlorides, bromides and triflates. useful ligand for the pd-catalyzed oxidation of alcohols in the presence of chlorobenzenes. useful ligand for the pd-catalyzed amination with ammonia equivalents. ligand for the gold(I)-catalyzed intramolecular [4+2] cycloadditions involving 1,3-enynes and arylalkynes with alkenes. ligand used in the palladium-catalyzed borylation of aryl bromdies. ligand used in the palladium-catalyzed siliylation of aryl chlorides. Additional or Alternative Names: Cyclohexyl JohnPhos. Product Category: Organic Phosphine Compounds. Appearance: Solid. CAS No. 247940-06-3. Molecular formula: C24H31P. Mole weight: 350.48. Purity: 0.98. IUPACName: dicyclohexyl-(2-phenylphenyl)phosphane. Canonical SMILES: C1CCC(CC1)P(C2CCCCC2)C3=CC=CC=C3C4=CC=CC=C4. ECNumber: 480-030-2. Product ID: ACM247940063-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4-Formylphenylboronic acid | Reagent used for: Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water ; Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides ; Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids ; Triethylamine-catalyzed three-component Hantzsch condensations ; Copper-catalyzed nitrations ; Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta ; Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides ; Palladium-catalyzed aerobic oxidative cross-coupling reactions Reagent used in Preparation of; Sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells; A novel protein synthesis inhibitor active against Gram-positive bacteria. Synonyms: Boronic acid, (4-formylphenyl)-; 4-Boronobenzaldehyde; p-formylphenylboronic acid; MFCD00151823; 4-benzaldehyde boronic acid; 4-(Dihydroxyboryl)benzaldehyde; CHEMBL140254. Grades: 95 %. CAS No. 87199-17-5. Molecular formula: C7H7BO3. Mole weight: 149.94. | |
| 4- (Vinyloxymethyl) cyclohexanemethanol | 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 |
| 5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine palladium(II) | 5,10,15,20-Tetrakis(pentafluorophenyl)-21H,23H-porphine palladium(II) is a phosphorescent dye that is a derivative of palladium(II). It can be used as a singlet oxygen sensitizer due to the presence of fluorine atoms. It provides photostability and is resistant to oxidation. Uses: It can be used as a porphyrin dye with a high quantum yield for use in the fabrication of oxygen sensors. Group: Organic field effect transistor (ofet) materials other materials. Alternative Names: Pd(II)meso-tetra(pentafluorophenyl) porphine. CAS No. 72076-09-6. Pack Sizes: 100 mg in glass insert. Product ID: palladium(2+); 5,10,15,20-tetrakis(2,3,4,5,6-pentafluorophenyl)porphyrin-22,24-diide. Molecular formula: 1078.9. Mole weight: C44H8F20N4Pd. C1=CC2=C (C3=NC (=C (C4=CC=C ([N-]4)C (=C5C=CC (=N5)C (=C1[N-]2)C6=C (C (=C (C (=C6F)F)F)F)F)C7=C (C (=C (C (=C7F)F)F)F)F)C8=C (C (=C (C (=C8F)F)F)F)F)C=C3)C9=C (C (=C (C (=C9F)F)F)F)F. [Pd+2]. InChI=1S/C44H8F20N4. Pd/c45-25-21 (26 (46)34 (54)41 (61)33 (25)53)17-9-1-2-10 (65-9)18 (22-27 (47)35 (55)42 (62)36 (56)28 (22)48)12-5-6-14 (67-12)20 (24-31 (51)39 (59)44 (64)40 (60)32 (24)52)16-8-7-15 (68-16)19 (13-4-3-11 (17)66-13)23-29 (49)37 (57)43 (63)38 (58)30 (23)50; /h1-8H; /q-2; +2. GRRRJZUTYPIXFO-UHFFFAOYSA-N. 98%+. | |
| Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II) | Allyl[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloropalladium(II). 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. Additional or 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)?-. Product Category: Organic Phosphine Compounds. Appearance: white solid. CAS No. 478980-03-9. Molecular formula: C30H42ClN2Pd. Mole weight: 572.54. Purity: 98%, Pd>18.5%. Product ID: ACM478980039. Alfa Chemistry ISO 9001:2015 Certified. | |
| Bathophenanthrolinedisulfonic acid disodium | Bathophenanthrolinedisulfonic acid disodium salt (BPS) is a colorimetric reagent for iron detection, with a wavelength of 535 nm for iron complex. It can be used for iron determination in aqueous solution systems without the need for extraction solvents. BPS can serve as a precursor to prepare Europium(III) tris(dibenzoylmethanate) bis(bathophenanthrolinedisulfonate) complex and ruthenium(II) tris (bathophenanthrolinedisulfonate), or participate in the catalytic oxidation of 2-hexanol by forming water-soluble complexes with palladium [1] [2] [3]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 52746-49-3. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W127790. |  |
| Biotinyl-phenylboronic acid | Biotinyl-phenylboronic acid is the functionalized arylboronic acid of biotin used for palladium-catalyzed oxidative Heck reaction to protein-bound alkenes and Suzuki-Miyaura cross-coupling for labeling of protein bound phenylhalides in high yields and with excellent chemoselectivity. Synonyms: [3-[5-(2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl)pentanoylamino]phenyl]boronic acid. Grades: 99%. CAS No. 1661014-48-7. Molecular formula: C16H22BN3O4S. Mole weight: 363.24. | |
| Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II) | Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II). Uses: Catalyst for: cross-coupling reactions. catalytic reduction reactions. preparation of silyl ethers via reaction of silicon-hydrogen bond with alcohols. oxidative carbonylation reactions. Additional or 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. Product Category: Palladium series catalysts. 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]. Product ID: ACM14267084. Alfa Chemistry ISO 9001:2015 Certified. | |
| (Oxybis(2,1-phenylene))bis(diphenylphosphine) | (Oxybis(2,1-phenylene))bis(diphenylphosphine). Uses: Useful as a ligand in the pd-catalyzed formation of diaryl amines. has been recently applied to the c3 benzylation of indoles. has been recently applied to the monoallylation of ammonia. ligand used in the palladium-catalyzed, aerobic oxidation coupling of acyl chlorides with arylboronic acids. ligand used in carbonylation of aryl iodides. ligand used in the direct c-h arylation of benzothiodiazoles. ligand used in stereo-retentive azacyclization of propargylic carbonates. ligand used in palladium catalyzed benzyne trimerization. Product Category: Organic Phosphine Compounds. CAS No. 166330-10-5. Molecular formula: C36H28OP2. Mole weight: 538.567g/mol. IUPACName: [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. Product ID: ACM166330105. Alfa Chemistry ISO 9001:2015 Certified. Categories: Bis[2-(diphenylphosphino)phenyl] Ether. | |
| Palladium | Palladium on carbon, often referred to as Pd/C, is a form of palladium used as a catalyst. The metal is supported on activated carbon in order to maximize its surface area and activity. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. the metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation. Additional or Alternative Names: ESCAT 1391;ESCAT 1371;ESCAT 1351;Paladium;PALLIDIUM. Appearance: Powder. CAS No. 7440-5-3. Molecular formula: Pd. Mole weight: 106.42. IUPACName: palladium. Canonical SMILES: [Pd]. Density: 1.025 g/mL at 25ºC. ECNumber: 231-115-6. Product ID: ACM7440053. Alfa Chemistry ISO 9001:2015 Certified. | |
| Palladium(II) acetate | Palladium(II) acetate. Uses: C-h activation; carbonylation; cross coupling reactions with arenes→mizoroki heck coupling reaction; cross coupling reactions with arenes→sonogashira-hagihara coupling reaction; cross coupling reactions with arenes→suzuki-miyaura coupling reaction; oxidation. Group: Solution deposition precursors. Alternative Names: Aceticacid,palladium(2+)salt. CAS No. 3375-31-3. Product ID: Palladium(2+); diacetate. Molecular formula: 224.51. Mole weight: C12H18O12Pd3. CC(=O)[O-].CC(=O)[O-].[Pd+2]. InChI=1S/2C2H4O2.Pd/c2*1-2(3)4; /h2*1H3, (H, 3, 4); /q; +2/p-2. YJVFFLUZDVXJQI-UHFFFAOYSA-L. 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: 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 on calcium carbonate | Palladium on calcium carbonate. Uses: Among the platinum group metals, palladium is the least noble metal, exhibiting greater reactivity than other metals of the group. the metal forms mostly bivalent compounds, although a small number of tetravalent and a fewer trivalent compounds are known. palladium exhibits a strong tendency to form complexes, most of which are four-coordinated square planar complexes of the metal in +2 oxidation. Group: Fuel cell catalysts. Product ID: calcium; palladium(2+); dicarbonate. Molecular formula: 266.5g/mol. Mole weight: C2CaO6Pd. C(=O)([O-])[O-]. C(=O)([O-])[O-]. [Ca+2]. [Pd+2]. InChI=1S/2CH2O3.Ca.Pd/c2*2-1(3)4; ; /h2*(H2, 2, 3, 4); ; /q; ; 2*+2/p-4. XGLHAVVVUOEGIO-UHFFFAOYSA-J. | |
| Tetrakis (triphenylphosphine)palladium (0) | Tetrakis (triphenylphosphine)palladium (0). Uses: Amination→buchwald-hartwig aminaton; carbonylation; cross coupling reactions with arenes→hiyama coupling reaction; cross coupling reactions with arenes→mizoroki heck coupling reaction; cross coupling reactions with arenes→negishi coupling reaction; cross coupling reactions with arenes→sonogashira-hagihara coupling reaction; cross coupling reactions with arenes→stille reaction; cross coupling reactions with arenes→suzuki-miyaura coupling reaction; cyclization; isomerization; oxidation; reduction. Group: Polymerization reagents. Alternative Names: tetrakis (triphenylphosphine) palladium(0); tetrakis (triphenylphosphine)-palladium(0); (Ph3P)4Pd; palladium (0) tetrakis (triphenylphosphine); EINECS 238-086-9; CTK5J6566; Tetrakis [triphenylphosphine]palladium (0) , ChemDose(TM) tablets, Loading: 2mumol per tablet; tetrakis(triphenylphosphine) palladium(0 ); M-5141; terakis (triphenylphosphine)palladium. CAS No. 14221-01-3. Product ID: palladium; triphenylphosphane. Molecular formula: 1155.58. Mole weight: C72H60P4Pd. 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. 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. [Pd]. InChI=1S/4C18H15P. Pd/c4*1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18; /h4*1-15H;. NFHFRUOZVGFOOS-UHFFFAOYSA-N. Metal | |
| Tris (dibenzylideneacetone)dipalladium (0) | Tris (dibenzylideneacetone)dipalladium (0). Uses: Amination→buchwald-hartwig aminaton; carbonylation; cross coupling reactions with arenes→mizoroki heck coupling reaction; cross coupling reactions with arenes→stille reaction; cross coupling reactions with arenes→suzuki-miyaura coupling reaction; oxidation; reduction. Group: Salt. Alternative Names: Bis[tris (dibenzylideneacetone)palladium (0)]. CAS No. 51364-51-3. Product ID: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium. Molecular formula: 915.73. Mole weight: C51H42O3Pd2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pd]. [Pd]. InChI=1S/3C17H14O. 2Pd/c3*18-17 (13-11-15-7-3-1-4-8-15) 14-12-16-9-5-2-6-10-16; /h3*1-14H; /b3*13-11+, 14-12+. CYPYTURSJDMMMP-WVCUSYJESA-N. 98%. | |
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