Rhodium Bromide Suppliers USA
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Product | Description | |
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Trans-dibromotetrakis(pyridine)rhodium bromide Quick inquiry Where to buy Suppliers range | Trans-dibromotetrakis(pyridine)rhodium bromide. Group: Rhodium Complexes. Alternative Names: (OC-6-12)-Dibromotetrakis (pyridine)rhodium (III) bromide. Grades: 97%. CAS No. 14267-74-4. Product ID: ACM14267744. Molecular formula: C20H20Br3N4Rh. Mole weight: 659.02. SMILES: C1=CC=NC=C1. C1=CC=NC=C1. C1=CC=NC=C1. C1=CC=NC=C1. [Br-]. [Br-]. [Br-]. [Rh+3]. | |
Rhodium (III) Bromide Quick inquiry Where to buy Suppliers range | RHODIUM (III) BROMIDE, HYDRATE, 99.9% pure, -60 mes, (Synonym: Rhodium Tribromide, Hydrate), Formula: RhBr3.xH2O. CAS No. 123333-87-9. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
Rhodium(III) bromide 2-hydrate Quick inquiry Where to buy Suppliers range | Rhodium(III) bromide 2-hydrate. Group: Rhodium Complexes. Alternative Names: Rhodium tribromide. CAS No. 15608-29-4. Molecular Weight: 342.62. Molecular Formula: Br3Rh. | |
(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. | |
2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl Quick inquiry Where to buy Suppliers range | 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl. Uses: Phosphine Ligand Kit component. Useful ligand for palladium-catalyzed carbon-nitrogen bond formation. Useful ligand for rhodium-catalyzed C-C bond formation. Useful ligand for palladium-catalyzed intramolecular acylation of aryl bromides via C-H activation. Used in the preparation of Buchwald third generation precatalyst. Used in methoxy directed Rhodium migration. Used in Nickel catalyzed C-N cross-coupling reactions. Group: Organic Phosphine Compounds. Alternative Names: F0001-2326; DB-009478; AC1LCPMX; (S)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL; AN-10356; SC-19338; (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene, puriss.; PubChem8136; TL8005203; (S)-(-)-2,2 inverted exclamation mark -Bis(diphenylphosphino)-1,1 inverted exclamation mark -binaphthalene. CAS No. 98327-87-8. Molecular formula: C44H32P2. Mole weight: 622.688g/mol. IUPAC Name: [1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Rotatable Bond Count: 7. Exact Mass: 622.198g/mol. EC Number: 616-304-7. SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. InChI: InChI=1S/C44H32P2/c1-5-19-35(20-6-1)45(36-21-7-2-8-22-36)41-31-29-33-17-13-15-27-39(33)43(41)44-40-28-16-14-18-34(40)30-32-42(44)46(37-23-9-3-10-24-37)38-25-11-4-12-26-38/h1-32H. InChIKey: MUALRAIOVNYAIW-UHFFFAOYSA-N. Monoisotopic Mass: 622.198g/mol. | |
Bis[η-(2,5-norbornadiene)]rhodium(I) Tetrafluoroborate Quick inquiry Where to buy Suppliers range | Bis[η-(2,5-norbornadiene)]rhodium(I) Tetrafluoroborate. Uses: Bis{P,P'-1,5-diphenyl-3,7-bis[(4-hydrogenphosphonate)phenyl]-1,5,3,7-diazadiphosphocine} nickel(II) bromide (hydrogen bromide adduct) can be used as Synthetic nickel catalyst used for photocatalytic reduction of aqueous protons to hydrogen and catalyst containing phosphonate anchor groups for immobilation on metal oxide semiconductor surfaces, enabling light-driven hydrogen evolution. Group: Rhodium series of catalysts. Alternative Names: 36620-11-8; Bis(norbornadiene)rhodium(I) tetrafluoroborate; [rh(nbd)2]bf4; SC-49716; Bis(bicyclo[2.2.1]hepta-2,5-diene)rhodium tetrafluoroborate; ANW-41403; MFCD00671775; Bis (norbornadiene) (tetrafluoroborato)rhodium; bis(norbomadiene)rhodium (I) tetrafluoroborate; Bis(norbornadiene)rhodium (I) tetrafluoroborate. CAS No. 36620-11-8. Molecular formula: C14H16BF4Rh-. Mole weight: 373.991g/mol. IUPAC Name: bicyclo[2.2.1]hepta-2,5-diene;rhodium;tetrafluoroborate. Exact Mass: 374.034g/mol. SMILES: [B-](F)(F)(F)F. C1C2C=CC1C=C2. C1C2C=CC1C=C2. [Rh]. InChI: InChI=1S/2C7H8.BF4.Rh/c2*1-2-7-4-3-6(1)5-7;2-1(3,4)5;/h2*1-4,6-7H,5H2;;/q;;-1; InChIKey: ZWPWNBFOFVFMPP-UHFFFAOYSA-N. H-Bond Acceptor: 5. Monoisotopic Mass: 374.034g/mol. | |
Bromotris(triphenylphosphine)rhodium Quick inquiry Where to buy Suppliers range | Bromotris(triphenylphosphine)rhodium. Uses: Rhodium-catalyzed regio- and stereoselective addition of diphenylphosphine oxide to alkynes. Rhodium- catalyzed hydrophosphinylation. Group: Rhodium series of catalysts. Alternative Names: bromide; Bromotris (triphenylphosphine)rhodium; EINECS 239-050-5; Bromotris (triphenylphosphine)rhodium (I); Jsp002843; phosphine, triphenyl-, bromide, rhodium salt(3:1); RL01906; AC1Q1R7U; triphenylphosphane. CAS No. 14973-89-8. Molecular formula: C54H45BrP3Rh-. Mole weight: 969.685g/mol. IUPAC Name: rhodium;triphenylphosphane;bromide. Rotatable Bond Count: 9. Exact Mass: 968.097g/mol. EC Number: 239-050-5. 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. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. [Rh]. InChI: InChI=1S/3C18H15P.BrH.Rh/c3*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;/h3*1-15H;1H;/p-1. InChIKey: HVQBRJSQQWBTDF-UHFFFAOYSA-M. H-Bond Acceptor: 1. Monoisotopic Mass: 968.097g/mol. | |
Bromotris (triphenylphosphine)rhodium (I) Quick inquiry Where to buy Suppliers range | Bromotris (triphenylphosphine)rhodium (I). Group: Rhodium Complexes. Alternative Names: Rhodium(I) tris(triphenylphosphine) bromide. Grades: 98%. CAS No. 14973-89-8. Product ID: ACM14973898-1. Molecular formula: C54H45BrP3Rh. Mole weight: 969.67. Appearance: Orange crystal. 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. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Br-]. [Rh]. |