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(E)-1-chloro-2-(3,3,3-trifluoroprop-1-en-1-yl)benzene is an organic chemical compound characterized by a benzene ring with a chlorine atom attached to the 1-position and a 3,3,3-trifluoroprop-1-en-1-yl group at the 2-position. This molecule features a double bond between the carbon atoms at the 1 and 2 positions, indicating the E-configuration, which means that the highest priority substituents are on opposite sides of the double bond. The trifluoroprop-1-en-1-yl group consists of a propene backbone with three fluorine atoms attached to the central carbon atom. (E)-1-chloro-2-(3,3,3-trifluoroprop-1-en-1-yl)benzene is known for its unique electronic properties and reactivity, which can be utilized in various chemical reactions and synthesis processes.

78622-60-3

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78622-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78622-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,6,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 78622-60:
(7*7)+(6*8)+(5*6)+(4*2)+(3*2)+(2*6)+(1*0)=153
153 % 10 = 3
So 78622-60-3 is a valid CAS Registry Number.

78622-60-3Downstream Products

78622-60-3Relevant academic research and scientific papers

Synthesis and Reactions of (2,2,2-Trifluoroethyl)triphenylphosphonium Trifluoromethanesulfonate

Hanamoto, Takeshi,Morita, Noriko,Shindo, Keiko

, p. 4279 - 4285 (2003)

(2,2,2-Trifluoroethyl)triphenylphosphonium trifluoromethanesulfonate (triflate) (1) was readily synthesized in high yield from triphenylphosphane and 2,2,2-trifluoroethyl triflate. The Wittig olefination of 1 with aromatic aldehydes bearing electron-withdrawing groups with CsF as a base in DMF proceeded cleanly, producing the corresponding 3,3,3-trifluoropropenylidene compounds in good yields. On the other hand, the hydrolysis of 1 in methanol containing sodium hydroxide gave (2,2-dimethoxyvinyl)triphenylphosphonium triflate (6a) in high yield instead of the corresponding (2,2,2-trifluoroethyl)diphenylphosphane oxide. Furthermore, reactions between 1 and secondary amines exclusively gave the novel (Z)-(2-amino-2-fluorovinyl)triphenylphosphonium triflates (10) in high yields. Wiley-VCH Verlag GmbH & Co KGaA, 69451 Weinheim, Germany, 2003.

Electrochemical Synthesis Strategy for Cvinyl-CF3 Compounds through Decarboxylative Trifluoromethylation

Hong, Huanliang,Li, Yibiao,Chen, Lu,Li, Bin,Zhu, Zhongzhi,Chen, Xiuwen,Chen, Ling,Huang, Yubing

, p. 5980 - 5986 (2019/05/10)

An efficient decarboxylative trifluoromethylation of α,β-unsaturated carboxylic acids using the Langlois reagent as a trifluoromethyl precursor has been achieved by an electro-oxidative strategy. Under catalyst-free and external oxidant-free electrolysis

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