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2-(2,6-dimethylphenyl)benzo[d]isothiazol-3(2H)-one, also known as 2,6-dimethylphenylbenzo[d]isothiazol-3(2H)-one, is a chemical compound with the molecular formula C15H13NOS. It is a derivative of benzo[d]isothiazol-3(2H)-one, featuring a 2,6-dimethylphenyl group attached to the 2-position of the benzo[d]isothiazol-3(2H)-one core. 2-(2,6-dimethylphenyl)benzo[d]isothiazol-3(2H)-one is often used as a reagent in various chemical reactions and can be found in research and development settings. Its structure and properties make it a valuable component in the synthesis of certain pharmaceuticals, agrochemicals, and other specialty chemicals.

4322-76-3

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4322-76-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4322-76-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,2 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4322-76:
(6*4)+(5*3)+(4*2)+(3*2)+(2*7)+(1*6)=73
73 % 10 = 3
So 4322-76-3 is a valid CAS Registry Number.

4322-76-3Downstream Products

4322-76-3Relevant academic research and scientific papers

An efficient approach to construct benzisothiazol-3(2: H)-ones via copper-catalyzed consecutive reaction of 2-halobenzamides and carbon disulfide

Li, Ting,Yang, Lei,Ni, Kaidong,Shi, Zhenyu,Li, Fei,Chen, Dongyin

, p. 6297 - 6303 (2016/07/11)

An efficient copper-catalyzed reaction for the synthesis of benzisothiazol-3(2H)-ones has been developed, starting from easily available 2-halobenzamides and carbon disulfide, which gave the corresponding target products in 30-89% yield for 25 examples. The reaction proceeds via a consecutive process with S-C bond and S-N bond formation.

Copper-catalyzed intramolecular N-S bond formation by oxidative dehydrogenative cyclization

Wang, Zhen,Kuninobu, Yoichiro,Kanai, Motomu

, p. 7337 - 7342 (2013/08/15)

Copper-catalyzed synthesis of benzo[d]isothiazol-3(2H)-ones and N-acyl-benzothiazetidine by intramolecular dehydrogenative cyclization is described. In this reaction, a new nitrogen-sulfur (N-S) bond is formed by N-H/S-H coupling. The present reaction has

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