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1-Bromo-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene is an organic chemical compound characterized by a benzene ring with a bromine atom attached at the 1st position and a 3,3,3-trifluoroprop-1-en-1-yl group at the 4th position. 1-bromo-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene is a halogenated aromatic compound, which means it contains a halogen (in this case, bromine) bonded to an aromatic ring. The presence of the trifluoroprop-1-en-1-yl group, which is a propene derivative with three fluorine atoms, adds to the compound's unique properties. It is likely to be used in the synthesis of more complex molecules, particularly in pharmaceuticals or materials science, due to its reactive sites and potential for further functionalization.

1983-12-6

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1983-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1983-12-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1983-12:
(6*1)+(5*9)+(4*8)+(3*3)+(2*1)+(1*2)=96
96 % 10 = 6
So 1983-12-6 is a valid CAS Registry Number.

1983-12-6Downstream Products

1983-12-6Relevant academic research and scientific papers

A Trifluoromethylcarbene Source

Duan, Yaya,Lin, Jin-Hong,Xiao, Ji-Chang,Gu, Yu-Cheng

, p. 2471 - 2474 (2016)

The trifluoromethylcarbene (:CHCF3) was found to be conveniently generated from (2,2,2-trifluoroethyl)diphenyl-sulfonium triflate (Ph2S+CH2CF3 -OTf), which was successfully applied in Fe-catalyzed cyclopropanation of olefins, giving the corresponding trifluoromethylated cyclopropanes in high yields.

Iodotrifluoromethylation of alkenes and alkynes with sodium trifluoromethanesulfinate and iodine pentoxide

Hang, Zhaojia,Li, Zejiang,Liu, Zhong-Quan

supporting information, p. 3648 - 3651 (2014/08/05)

A scalable, selective, and operationally easy iodotrifluoromethylation of a wide range of alkenes and alkynes by using two simple and safe solids, sodium trifluoromethanesulfinate and iodine pentoxide, in aqueous medium has been developed. Mechanistic studies confirm that free-radical processes are involved in this system since the key radical intermediates such as CF3 and β-CF3 alkyl radicals have been clearly detected by spin trapping and electron spin resonance.

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