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benzyl (2,3,5,6-tetrafluorophenyl)sulfane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1376608-47-7

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1376608-47-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1376608-47-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,6,6,0 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1376608-47:
(9*1)+(8*3)+(7*7)+(6*6)+(5*6)+(4*0)+(3*8)+(2*4)+(1*7)=187
187 % 10 = 7
So 1376608-47-7 is a valid CAS Registry Number.

1376608-47-7Relevant academic research and scientific papers

Synthesis of polyfluorinated aromatic ethers and thioethers by synergistic cleavage of C-B bond and C-F bond of B(C6F5)3

Ma, Cui-Cui,Zhu, Xing-Xing,Liu, Li,Dai, Jian-Jun,Xu, Jun,Xu, Hua-Jian

supporting information, (2021/09/11)

A concise and efficient method for the synthesis of polyfluorinated aromatic ethers and thioethers by synergistic cleavage of C-B bond and C-F bond of B(C6F5)3 is reported. The reaction could proceed smoothly with excellent functional-group compatibility. In addition, the transformation represents the first general application of B(C6F5)3 as reaction partners in cross-coupling reaction.

2-ARYLSULFONAMIDO-N-ARYLACETAMIDE DERIVATIZED STAT3 INHIBITORS

-

Paragraph 00936; 00938, (2018/08/20)

The present disclosure provides pharmaceutical compositions comprising 2-arylsulfonamido-N-arylacetamide derivatized Stat3 inhibitors and certain pharmaceutically acceptable salts thereof, and methods of their use.

Regioselective C-S bond formation accomplished by copper-catalyzed regioselective C-F substitution of perfluoroarenes with aryl thioacetates or benzyl thioacetate

Zhou, Qizhong,Zhang, Bin,Du, Tieqi,Gu, Haining,Jiang, Huajiang,Chen, Rener

experimental part, p. 4233 - 4241 (2012/07/14)

Practical and straightforward method for regioselective C-S bond formation accomplished by copper-catalyzed regioselective C-F substitution of electron-deficient perfluoroarenes with aryl thioacetates or benzyl thioacetate has been developed. Because of its high reaction efficiency, good chemoselectivity and regioselectivity, and excellent functional-group compatibility, this protocol provides a useful and operationally simple access to polyfluoroaryl thioethers used for drugs and material chemistry.

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