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145914-06-3

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145914-06-3 Usage

Physical state

Colorless liquid

Uses

a. Intermediate in the synthesis of pharmaceuticals and agrochemicals
b. Production of dyes and pigments
c. Manufacture of other specialty chemicals

Environmental impact

Potent greenhouse gas

Contribution to global warming

Significant

Regulatory status

Use and production regulated in many countries to mitigate environmental impact

Check Digit Verification of cas no

The CAS Registry Mumber 145914-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,9,1 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 145914-06:
(8*1)+(7*4)+(6*5)+(5*9)+(4*1)+(3*4)+(2*0)+(1*6)=133
133 % 10 = 3
So 145914-06-3 is a valid CAS Registry Number.

145914-06-3Downstream Products

145914-06-3Relevant articles and documents

Metal-Free Construction of the C(sp3)-CF3 Bond: Trifluoromethylation of Hydrazones with Togni's Reagent under Mild Conditions

Zeng, Huiying,Luo, Zhen,Han, Xinlong,Li, Chao-Jun

supporting information, p. 5948 - 5951 (2019/08/29)

A metal-free trifluoromethylation of hydrazones with Togni's reagent under mild conditions was developed. Various functional groups including ester, methoxy, dimethoxy, nitro, halogen, and heterocyclic compounds were tolerated. This simple and green strategy provides a practical tool to construct C(sp3)-CF3 bonds.

A facile synthesis of isomeric C -(2,2,2-trifluoroethyl)anilines

Trofymchuk, Sergii,Bezdudny, Andrii V.,Pustovit, Yurii M.,Lukin, Oleg,Boyko, Alexander N.,Chekotylo, Alexey,Tolmachev, Andrei A.,Mykhailiuk, Pavel K.

experimental part, p. 1974 - 1976 (2012/08/27)

Three isomers of C-(2,2,2-trifluoroethyl)aniline were prepared on a multigram scale from readily available nitrophenylacetic acids in two steps. First, the carboxy groups of the latter were converted into the trifluoromethyl moieties by treatment with sul

The reactions of copper-dibromodifluoromethane-amide systems with alcohols

Clark, James H.,McClinton, Martin A.,Blade, Robert J.

, p. 257 - 267 (2007/10/02)

1,1,1-Trifluoro-2-arylethanes can be prepared by the trifluoromethyldehydroxylation of benzyl alcohols using the copper-dibromodifluoromethane-amide reaction system, although the yields are low.The mechanism of the reaction may involve chelation of the substrate to copper so that α-substituted benzyl alcohols and other alcohols are unreactive.

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