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4-((2-chlorophenyl)thio)aniline, also known as 2-chloro-4'-aminodiphenyl sulfide, is an organic compound with the chemical formula C12H10ClNS. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. 4-((2-chlorophenyl)thio)aniline is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is used in the production of herbicides, fungicides, and other chemical products. Due to its reactivity, it is essential to handle 4-((2-chlorophenyl)thio)aniline with care, as it may pose health risks and environmental concerns.

4726-27-6

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4726-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4726-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4726-27:
(6*4)+(5*7)+(4*2)+(3*6)+(2*2)+(1*7)=96
96 % 10 = 6
So 4726-27-6 is a valid CAS Registry Number.

4726-27-6Downstream Products

4726-27-6Relevant academic research and scientific papers

Iodine/DMSO-Promoted Selective Direct Arylthiation of Anilines with Thiols under Metal-Free Conditions

Zhao, Wenqi,Zhang, Feng,Deng, Guo-Jun

, p. 291 - 301 (2021/01/14)

An iodine-promoted divergent thiolation of unprotected anilines with thiols for the synthesis of sulfide anilines has been described. The combinational use of I2 and DMSO played an important role to realize this kind of transformation without the aid of a

Flavin/I2 catalyzed aerobic oxidative C–H sulfenylation of anilines

Jiang, Xinpeng,Shen, Zhifeng,Zheng, Cong,Fang, Liyun,Chen, Keda,Yu, Chuanming

supporting information, (2020/07/24)

A flavin/I2 catalyzed aerobic oxidative C–H sulfenylation of anilines with thiols under mild reaction conditions is presented for the first time. This metal-free reaction provides an atom-economic pathway to prepare various aryl sulfides with outstanding functional group compatibility. Moreover, it consumes molecular oxygen as the only terminal oxidant and produces environmentally-friendly H2O as the only byproduct.

Structure-based design of substituted diphenyl sulfones and sulfoxides as lipophilic inhibitors of thymidylate synthase

Jones, Terence R.,Webber, Stephen E.,Varney, Michael D.,Reddy, M. Rami,Lewis, Kathleen K.,Kathardekar, Vinit,Mazdiyasni, Hormoz,Deal, Judith,Nguyen, Dzuy,Welsh, Katharine M.,Webber, Stephanie,Johnston, Amanda,Matthews, David A.,Smith, Ward W.,Janson, Cheryl A.,Bacquet, Russell J.,Howland, Eleanor F.,Booth, Carol L. J.,Herrmann, Steven M.,Ward, Robert W.,White, Jennifer,Bartlett, Charlotte A.,Morse, Cathy A.

, p. 677 - 683 (2007/10/03)

Six new diphenyl sulfoxide and five new diphenyl sulfones were designed, synthesized, and tested for their inhibition of human and Escherichia coli thymidylate synthase (TS) and of the growth of cells in tissue culture. The best sulfoxide inhibitor of hum

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