800-67-9

Basic information

• Product Name: 1-{(2-[3-trifluoromethyl)phenyl]-1-phenylvinyl}benzene
• Synonyms: 1-{(2-[3-trifluoromethyl)phenyl]-1-phenylvinyl}benzene
• CAS NO: 800-67-9
• Molecular Weight: 324.345
• Mol File: 800-67-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-{(2-[3-trifluoromethyl)phenyl]-1-phenylvinyl}benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{(2-[3-trifluoromethyl)phenyl]-1-phenylvinyl}benzene(800-67-9)
• EPA Substance Registry System: 1-{(2-[3-trifluoromethyl)phenyl]-1-phenylvinyl}benzene(800-67-9)

Safety Data

• Hazardous Substances Data: 800-67-9(Hazardous Substances Data)

Upstream product

• 635305-32-7 5,5-dimethyl-2-(3-(trifluoromethyl)phenyl)-1,3,2-dioxaborinane 
• 40237-72-7 (2-methoxyethene-1,1-diyl)dibenzene 
• 98-80-6 phenylboronic acid 
• 98-81-7 1-bromovinylbenzene 
• 947-91-1 Diphenylacetaldehyde 
• 2923-40-2 [m-(trifluoromethyl)phenyl]magnesium chloride 
• 28075-38-9 (2,2-diphenylvinyl)trifluoromethnesulfonate 
• 530-48-3 1,1-Diphenylethylene 
• 401-78-5 3-bromo-1-trifluoromethylbenzene 
• 119-61-9 benzophenone 
• 705-29-3 3-Trifluoromethylbenzyl chloride 

Downstream Products

• 802-02-8 2-Brom-1,1-diphenyl-2-<3-trifluormethyl-phenyl>-aethylen 

Relevant articles and documents

Nickel-catalyzed cross-coupling reaction of alkenyl methyl ethers with aryl boronic esters

The Ni(0)-catalyzed cross-coupling of alkenyl methyl ethers with boronic esters is described. Several types of alkenyl methyl ethers can be coupled with a wide range of boronic esters to give the stilbene derivatives.

Synthesis of polysubstituted alkenes by Heck vinylation or Suzuki cross-coupling reactions in the presence of a tetraphosphane-palladium catalyst

Through the use of [PdCl(C3H5)]2/cis,cis,cis-1,2,3, 4-tetrakis[(diphenylphosphanyl)methyl]cyclopentane as a catalyst, a range of vinyl bromides undergo Suzuki cross-couplings with arylboronic acids in good yields. Furthermore, the catalyst can be used at low loadings, even for reactions of sterically hindered substrates. Mediated by this catalyst, stilbene and 1,1-diphenylethylene undergo Heck reactions with aryl halides to give triarylethylene derivatives. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.