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Cy-vBRIDP

Catalog Number
ACM384842244-2
Product Name
Cy-vBRIDP
Structure
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CAS
384842-24-4
  • Product Overview
  • Usage
Synonyms
AKOS025295265; Acm³84842244; CTK8E6999; 1,1-Diphenyl-2-(dicyclohexylphosphino)propene; 1-Methyl-2,2-diphenylvinyldicyclohexylphosphine; Cy-vBRIDP; 2-(Dicyclohexylphosphino)-1,1-diphenyl-1-propene, Dicyclohexyl(1-methyl-2,2-diphenylvinyl)phosphine; Cy-vBRIDP(regR); DTXSID40475778; DICYCLOHEXYL(1-METHYL-2,2-DIPHENYLVINYL)PHOSPHINE;
IUPAC Name
dicyclohexyl(1,1-diphenylprop-1-en-2-yl)phosphane;
Molecular Weight
390.551g/mol
Molecular Formula
C27H35P;
Canonical SMILES
CC(=C(C1=CC=CC=C1)C2=CC=CC=C2)P(C3CCCCC3)C4CCCCC4;
InChI
InChI=1S/C27H35P/c1-22(27(23-14-6-2-7-15-23)24-16-8-3-9-17-24)28(25-18-10-4-11-19-25)26-20-12-5-13-21-26/h2-3,6-9,14-17,25-26H,4-5,10-13,18-21H2,1H3;
InChI Key
YMSBPYCREGBACF-UHFFFAOYSA-N;
Storage
2-8°C
Complexity
444
Covalently-Bonded Unit Count
1
Exact Mass
390.248g/mol
Heavy Atom Count
28
Monoisotopic Mass
390.248g/mol
Rotatable Bond Count
5
Topological Polar Surface Area
0A^2
Application
Cy-vBRIDP is designed to facilitate and enhance chemical reactions, serving as a versatile catalyst particularly in cycloaddition reactions. It functions as an effective ligand in palladium-catalyzed amination of aryl halides, playing a critical role in forming new chemical bonds. Additionally, Cy-vBRIDP is utilized in Suzuki-Miyaura coupling, contributing to the efficient synthesis of biaryls and complex organic molecules, making it an invaluable tool in the field of organic chemistry.
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