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4,4,4-trifluoro-2-(2-chlorophenyl)-1-(4-chlorophenyl)butan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1448819-62-2

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1448819-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448819-62-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,8,1 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1448819-62:
(9*1)+(8*4)+(7*4)+(6*8)+(5*8)+(4*1)+(3*9)+(2*6)+(1*2)=202
202 % 10 = 2
So 1448819-62-2 is a valid CAS Registry Number.

1448819-62-2Downstream Products

1448819-62-2Relevant academic research and scientific papers

NHC-Catalyzed Radical Trifluoromethylation Enabled by Togni Reagent

Zhang, Bei,Peng, Qiupeng,Guo, Donghui,Wang, Jian

, p. 443 - 447 (2020)

An unprecedented carbene-catalyzed radical trifluoromethylation of olefins with aldehydes in the presence of Togni reagent was developed, thus providing the β-trifluoromethyl-α-substituted ketones with a broad scope and moderate to high chemical yields. Notably, this process includes a single-electron-transfer process and utilizes the persistent N-heterocyclic-carbene-bound radical as a key intermediate to trigger the cascade radical cross-coupling.

Iron-catalyzed trifluoromethylation with concomitant C-C bond formation via 1,2-migration of an aryl group

Egami, Hiromichi,Shimizu, Ryo,Usui, Yoshihiko,Sodeoka, Mikiko

supporting information, p. 7346 - 7348 (2013/09/23)

Iron-catalyzed trifluoromethylation with concomitant 1,2-migration of an aryl group starting from diaryl allyl alcohol was achieved under mild conditions. This reaction system affords α-substituted-β- trifluoromethyl carbonyl compounds in high efficiency.

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