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

54043-37-7

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54043-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54043-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,0,4 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54043-37:
(7*5)+(6*4)+(5*0)+(4*4)+(3*3)+(2*3)+(1*7)=97
97 % 10 = 7
So 54043-37-7 is a valid CAS Registry Number.

54043-37-7Downstream Products

54043-37-7Relevant academic research and scientific papers

Carbotrifluoromethylation of Allylic Alcohols via 1,2-Aryl Migration Promoted by Visible-Light-Induced Photoredox Catalysis

Cai, Shunyou,Tian, Yu,Zhang, Jinwang,Liu, Zhiji,Lu, Maojian,Weng, Wen,Huang, Mingqiang

, p. 4084 - 4088 (2018)

Visible-light-enabled photocatalytic carbotrifluoro-methylations of allylic alcohols and sodium triflinate were explored through 1,2-migration of an aryl group, affording an efficient method for synthesis of β-trifluoromethyl-α-substituted carbonyl compou

Electrochemical Oxidative Aryl(alkyl)trifluoromethylation of Allyl Alcohols via 1,2-Migration

Guan, Zhipeng,Wang, Huamin,Huang, Yange,Wang, Yunkun,Wang, Shengchun,Lei, Aiwen

supporting information, p. 4619 - 4622 (2019/06/17)

An electrochemical oxidative difunctionalization of allyl alcohols for the synthesis of β-trifluoromethyl ketones is achieved through a 1,2-migration process. A series of β-trifluoromethyl ketones can be facilely obtained utilizing CF3SO2

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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