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S-Methyl 4-cyanobenzothioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

536708-67-5

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536708-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 536708-67-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,6,7,0 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 536708-67:
(8*5)+(7*3)+(6*6)+(5*7)+(4*0)+(3*8)+(2*6)+(1*7)=175
175 % 10 = 5
So 536708-67-5 is a valid CAS Registry Number.

536708-67-5Relevant academic research and scientific papers

Palladium Catalyzed Direct Carbonylative Thiomethylation of Aryldiazonium Salts and Amines with 4-(Methylthio)-2-Butanone as (Methylthio) Transfer Agent

Tian, Qingqiang,Xu, Shasha,Zhang, Chiying,Liu, Xinyi,Wu, Xiangwei,Li, Yahui

, p. 8797 - 8804 (2021/07/19)

Herein, an interesting palladium-catalyzed procedure for the direct carbonylative thiomethylation of aromatic amine derivatives with 4-methylthio-2-butanone is developed. Using 4-methylthio-2-butanone as (methylthio) transfer agent, a variety of corresponding thioesters are obtained with moderate to good yields under base-free condition. In addition, good functional group tolerance can be observed.

Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters

Li, Yahui,Bao, Gao,Wu, Xiao-Feng

, p. 2187 - 2192 (2020/03/11)

Functional group transfer reactions are an important synthetic tool in modern organic synthesis. Herein, we developed a new palladium-catalyzed intermolecular transthioetherification reaction of aryl halides with thioethers and thioesters. The synthetic utility and practicality of this catalytic protocol are demonstrated in a wide range of successful transformations (>70 examples). This catalytic protocol is applicable in carbonylative coupling processes as well, and the first example of carbonylative methylthioesterification of aryl halides has been achieved. Notably, this work also provides an approach to using natural products, such as methionine and selenomethionine, as the functional group sources.

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