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Ethanone, 2-[(4-bromophenyl)sulfonyl]-1-(2-thienyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193469-57-7

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193469-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193469-57-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,6 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 193469-57:
(8*1)+(7*9)+(6*3)+(5*4)+(4*6)+(3*9)+(2*5)+(1*7)=177
177 % 10 = 7
So 193469-57-7 is a valid CAS Registry Number.

193469-57-7Downstream Products

193469-57-7Relevant academic research and scientific papers

An efficient access to β-ketosulfones: Via β-sulfonylvinylamines: Metal-organic framework catalysis for the direct C-S coupling of sodium sulfinates with oxime acetates

To, Tuong A.,Tran, Chau B.,Nguyen, Ngoc T. H.,Nguyen, Hai H. T.,Nguyen, Anh T.,Phan, Anh N. Q.,Phan, Nam T. S.

, p. 17477 - 17485 (2018)

A copper-based framework Cu2(OBA)2(BPY) was synthesized and used as a recyclable heterogeneous catalyst for the synthesis of β-sulfonylvinylamines from sodium sulfinates and oxime acetates via direct C-S coupling reaction. The transformation was remarkably affected by the solvent, and chlorobenzene emerged as the best option. This Cu-MOF displayed higher activity than numerous conventional homogeneous and MOF-based catalysts. The catalyst was reutilized many times in the synthesis of β-sulfonylvinylamines without considerably deteriorating in catalytic efficiency. These β-sulfonylvinylamines were readily converted to the corresponding β-ketosulfones via a hydrolysis step with aqueous HCl solution. To the best of our knowledge, this direct C-S coupling reaction to achieve β-sulfonylvinylamines was not previously conducted with a heterogeneous catalyst.

CHEMICAL COMPOUNDS

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Page 104, (2010/02/06)

Compounds of formula (I):wherein variable groups are as defined within; for use in the inhibition of 11betaHSD1 are described

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