| Identification | Back Directory | [Name]
[2',4'-Bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexylphosphine | [CAS]
1848244-75-6 | [Synonyms]
phosphino-2'-methoxy-4',6'-di-t-butyL
2-Dicyclohexylphosphino-2'-methoxy-4',6'-di-t-buty
2-Dicyclohexylphosphino-2′-methoxy-4′,6′-di-tert-butylbiphenyl
2-Dicyclohexylphosphino-2'-methoxy-4',6'-di-t-butyl-1,1'-biphenyl
2-Dicyclohexylphosphino-2'-methoxy-4',6'-di-t-butyl-1,1'-biphenyl, Vphos
2',4' -di-tert-butyl-6 '-methoxy-1,1' -biphenyl -2-dicyclohexylphosphine
Dicyclohexyl(2',4'-di-tert-butyl-6'-methoxy-[1,1'-biphenyl]-2-yl)phosphane
2-Dicyclohexylphosphino-2'-methoxy-4',6'-di-t-butyl-1,1'-biphenyl,min.98%VPhos
[2',4'-Bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexylphosphine
Phosphine, [2',4'-bis(1,1-dimethylethyl)-6'-methoxy[1,1'-biphenyl]-2-yl]dicyclohexyl- | [Molecular Formula]
C33H49OP | [MDL Number]
MFCD30184625 | [MOL File]
1848244-75-6.mol | [Molecular Weight]
492.72 |
| Chemical Properties | Back Directory | [Melting point ]
113-118 °C | [Boiling point ]
561.5±50.0 °C(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [form ]
solid | [color ]
white to off-white | [InChI]
1S/C33H49OP/c1-32(2,3)24-22-28(33(4,5)6)31(29(23-24)34-7)27-20-14-15-21-30(27)35(25-16-10-8-11-17-25)26-18-12-9-13-19-26/h14-15,20-23,25-26H,8-13,16-19H2,1-7H3 | [InChIKey]
LYVFKWGKMKCNPE-UHFFFAOYSA-N | [SMILES]
P(C1=CC=CC=C1C1=C(OC)C=C(C(C)(C)C)C=C1C(C)(C)C)(C1CCCCC1)C1CCCCC1 |
| Hazard Information | Back Directory | [Uses]
As the Pd G4 complex, this ligand from the Buchwald group offers best-in-class performance in the micellar aqueous Negishi coupling of heterocyclic alkyl bromides. | [reaction suitability]
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
reaction type: Cross Couplings
reagent type: ligand
reaction type: click chemistry |
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