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1571792-29-4

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1571792-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1571792-29-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,1,7,9 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1571792-29:
(9*1)+(8*5)+(7*7)+(6*1)+(5*7)+(4*9)+(3*2)+(2*2)+(1*9)=194
194 % 10 = 4
So 1571792-29-4 is a valid CAS Registry Number.

1571792-29-4Downstream Products

1571792-29-4Relevant articles and documents

Intramolecular Mizoroki-Heck Reaction of 2-Thiosubstituted Acrylates for the Synthesis of 3-Substituted Benzo[ b ]thiophene-2-carboxylates

Kwak, Se Hun,Lim, Su-Jeong,Yoo, Hyun-Jeong,Ha, Ji-Eun,Gong, Young-Dae

, p. 4131 - 4142 (2016)

3-Substituted 2-(phenylthio)acrylates prepared from aldol condensation using titanium tetrachloride were employed to synthesize benzo[b]thiophenes. The acrylates containing aryls and alkyls generated the desired benzo[b]thiophenes in reasonable yields und

Visible-light-induced decarboxylative sulfonylation of cinnamic acids with sodium sulfinates by using Merrifield resin supported Rose Bengal as a catalyst

Li, Pinhua,Wang, Guan-Wu

supporting information, p. 5578 - 5585 (2019/06/13)

A visible-light-induced decarboxylative sulfonylation of cinnamic acids with sodium sulfinates for the synthesis of vinyl sulfones was developed. The reaction proceeded smoothly in the presence of Merrifield resin supported Rose Bengal ammonium salt as a

Copper-catalyzed highly selective direct hydrosulfonylation of alkynes with arylsulfinic acids leading to vinyl sulfones

Wei, Wei,Li, Jinli,Yang, Daoshan,Wen, Jiangwei,Jiao, Yueting,You, Jinmao,Wang, Hua

, p. 1861 - 1864 (2014/03/21)

A novel Cu-catalyzed direct hydrosulfonylation of alkynes with arylsulfinic acids for the synthesis of (E)-vinyl sulfones has been realized under mild conditions with 100% atom efficiency. The present protocol provides an attractive approach to various vinyl sulfones in good to excellent yields, with the advantages of operation simplicity, atom economy, and high stereo- and regioselectivities.

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