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1-{(2-[3-trifluoromethyl)phenyl]-1-phenylvinyl}benzene is a complex organic compound characterized by its unique molecular structure. It consists of a benzene ring with a phenyl group attached to it, which in turn is connected to another phenyl group through a vinyl bond. The second phenyl group has a trifluoromethyl substituent at the 3-position, which imparts specific chemical properties to the molecule. 1-{(2-[3-trifluoromethyl)phenyl]-1-phenylvinyl}benzene is known for its potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its unique electronic and steric properties. The presence of the trifluoromethyl group can significantly influence the molecule's reactivity, stability, and lipophilicity, making it an interesting target for synthetic chemists and researchers in the field of organic chemistry.

800-67-9

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800-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 800-67-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,0 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 800-67:
(5*8)+(4*0)+(3*0)+(2*6)+(1*7)=59
59 % 10 = 9
So 800-67-9 is a valid CAS Registry Number.

800-67-9Relevant academic research and scientific papers

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

Shimasaki, Toshiaki,Konno, Yuko,Tobisu, Mamoru,Chatani, Naoto

supporting information; experimental part, p. 4890 - 4892 (2010/01/06)

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.

Iron-catalyzed cross-coupling between alkenyl and dienyl sulfonates and functionalized arylcopper reagents

Dunet, Guillaume,Knochel, Paul

, p. 407 - 410 (2007/10/03)

Functionalized arylcopper reagents react readily with alkenyl sulfonates in the presence of catalytic amounts of Fe(acac)3, (10 mol%) providing the expected cross-coupling products in good yields. Ester or cyano group are tolerated. This cross-coupling can be performed with dienyl sulfonates leading to the corresponding substituted dienes. Georg Thieme Verlag Stuttgart.

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

Berthiol, Florian,Doucet, Henri,Santelli, Maurice

, p. 1091 - 1096 (2007/10/03)

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.

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