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Methanesulfonic acid, trifluoro-, 1-(3-chlorophenyl)ethenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56039-41-9

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56039-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56039-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,0,3 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 56039-41:
(7*5)+(6*6)+(5*0)+(4*3)+(3*9)+(2*4)+(1*1)=119
119 % 10 = 9
So 56039-41-9 is a valid CAS Registry Number.

56039-41-9Downstream Products

56039-41-9Relevant academic research and scientific papers

Radical Desulfur-Fragmentation and Reconstruction of Enol Triflates: Facile Access to α-Trifluoromethyl Ketones

Su, Xiaolong,Huang, Honggui,Yuan, Yaofeng,Li, Yi

, p. 1338 - 1341 (2017)

We report an efficient oxidative radical desulfur-fragmentation and reconstruction of enol triflates for the synthesis of α-CF3ketones. Preliminary mechanistic studies disclosed that oxidative fragmentation to release a CF3radical fr

Chemoselective Synthesis of 1,1-Disubstituted Vinyl Triflates from Terminal Alkynes Using TfOH in the Presence of TMSN3

Tummatorn, Jumreang,Punjajom, Kunlayanee,Rodphon, Warabhorn,Ruengsangtongkul, Sureeporn,Chaisan, Nattawadee,Lumyong, Kanyapat,Thongsornkleeb, Charnsak,Nimnual, Phongprapan,Ruchirawat, Somsak

supporting information, p. 4694 - 4697 (2019/06/27)

1,1-Disubstituted vinyl triflates are synthesized by direct hydrotriflation of terminal alkynes employing a combination of TfOH and TMSN3 in DCM at room temperature. Interestingly, under these conditions, only terminal alkynes were selectively

Visible light induced Trifluoromethyl Migration: Easy Access to α-Trifluoromethylated Ketones from Enol Triflates

Liu, Shuyang,Jie, Jiyang,Yu, Jipan,Yang, Xiaobo

supporting information, p. 267 - 271 (2017/11/13)

Herein, we reported a novel method to synthesize α-trifluoromethylated ketones from enol triflates. Involving a cascade sulfur dioxide extrusion and a CF3 (trifluoromethyl) radical addition process, this reaction proceeds at room temperature an

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