Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine Cy-cBRIDP
Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine Cy-cBRIDP Basic information
- Product Name:
- Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine Cy-cBRIDP
- Synonyms:
-
- Cy-cBRIDP(regR)
- Cy-cBRIDP 97%
- Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine
- Cy-cBRIDP®
- Cy-cBRIDP[R]
- Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine Cy-cBRIDP
- dicyclohexyl-(1-methyl-2,2-diphenylcyclopropyl)phosphane
- Cy-cBRIDP(regR) >
- CAS:
- 1023330-38-2
- MF:
- C28H37P
- MW:
- 404.57
- Product Categories:
-
- Achiral Phosphine
- Aryl Phosphine
- organophosphine ligand
- Mol File:
- 1023330-38-2.mol
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Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine Cy-cBRIDP Chemical Properties
- Melting point:
- 115-122°C
- storage temp.
- 2-8°C
- form
- solid
- color
- white to pale yellow
- Sensitive
- air sensitive, store cold
- CAS DataBase Reference
- 1023330-38-2
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Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine Cy-cBRIDP Usage And Synthesis
Reaction
- Ligand effective for many classes of palladium-catalyzed coupling of aryl halides, including the Miyaura-Suzuki, BuchwaldHartwig, Sonogashira, Heck, aryl etherification, and carbonylation reactions.
- Ligand used in the palladium catalyzed Suzuki-Miyaura coupling of aryl boronic acids.
- Ligand employed in the palladium-catalyzed Buchwald-Hartwig aryl amination reaction.
Uses
Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine can be used as a catalyst.
Uses
Takasago Ligands and Complexes for Asymmetric Reactions
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: ligand
Dicyclohexyl(2,2-diphenyl-1-methylcyclopropyl)phosphine Cy-cBRIDPSupplier
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