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1-(2-bromo-1-phenylvinyl)-4-(trifluoromethyl)benzene is an organic compound characterized by a unique molecular structure. It features a benzene ring with a trifluoromethyl group at the 4-position, which imparts electron-withdrawing properties. Additionally, the molecule contains a vinyl group (C=C) attached to the 1-position of the benzene ring, which is further substituted with a 2-bromo-1-phenyl group. This bromine atom and phenyl ring at the vinyl position introduce a significant steric and electronic influence on the molecule. The combination of these functional groups results in a compound with potential applications in various chemical and pharmaceutical processes, such as the synthesis of complex organic molecules and intermediates. The specific arrangement of atoms and the presence of halogen and aromatic rings make 1-(2-bromo-1-phenylvinyl)-4-(trifluoromethyl)benzene a subject of interest in organic chemistry, particularly for its reactivity and potential use in the formation of new chemical bonds.

365-09-3

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365-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 365-09-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,6 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 365-09:
(5*3)+(4*6)+(3*5)+(2*0)+(1*9)=63
63 % 10 = 3
So 365-09-3 is a valid CAS Registry Number.

365-09-3Downstream Products

365-09-3Relevant academic research and scientific papers

Halogenation of 1,1-diarylethylenes by N-halosuccinimides

Zhang, Ge,Bai, Rui-Xue,Li, Chu-Han,Feng, Chen-Guo,Lin, Guo-Qiang

, p. 1658 - 1662 (2018/12/11)

An efficient method for the preparation of 2,2-diarylvinyl halides from the corresponding 1,1-diarylethylenes has been developed. N-Halosuccinimides (N-bromosuccinimide or N-chlorosuccinimide) were used as the halogenation reagents. The practicability of this method is highlighted by its simple operation, broad substrate scope and capability for large-scale reaction.

A kinetic, product and kinetic isotope effect investigation of the bromination of 1,1-diphenylethyIenes and of their 2,2-dideuterio derivatives

Bellucci, Giuseppe,Chiappe, Cinzia

, p. 581 - 584 (2007/10/03)

The kinetics of bromination of 1,1-diphenylethylene (1a), 4-trifluoromethyl-1,1-diphenylethylene (1b), and 1-(3-trifluoromethylphenyl)-1-(4-trifluoromethylphenyl)ethylene (1c) and of their 2,2-dideuterio derivatives have been investigated in 1,2-dichloroe

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