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(3R)-tert-butyl 3-(2-(3-chlorophenyl)-2-oxoethyl)-3-hydroxy-2-oxo-2,3-dihydro-1H-indoline-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1392149-64-2

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1392149-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1392149-64-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,1,4 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1392149-64:
(9*1)+(8*3)+(7*9)+(6*2)+(5*1)+(4*4)+(3*9)+(2*6)+(1*4)=172
172 % 10 = 2
So 1392149-64-2 is a valid CAS Registry Number.

1392149-64-2Downstream Products

1392149-64-2Relevant academic research and scientific papers

Enantioselective decarboxylative aldol addition of β-ketoacids to isatins catalyzed by binaphthyl-modified organocatalyst

Suh, Chang Won,Chang, Chul Woo,Choi, Keon Woong,Lim, Young Jo,Kim, Dae Young

, p. 3651 - 3654 (2013/07/05)

The catalytic enantioselective decarboxylative aldol addition reaction of isatins with β-ketoacids promoted by chiral bifunctional organocatalysts have been developed, allowing facile synthesis of the corresponding chiral 3-hydroxy-3-phenacyloxindole deri

Enantioselective construction of 3-hydroxy oxindoles via decarboxylative addition of β-ketoacids to isatins

Zhong, Fangrui,Yao, Weijun,Dou, Xiaowei,Lu, Yixin

supporting information; experimental part, p. 4018 - 4021 (2012/09/21)

The first highly enantioselective decarboxylative addition of β-ketoacids to isatins mediated by a bifunctional tertiary amine-thiourea catalyst has been developed, allowing facile synthesis of biologically important 3-hydroxy oxindoles in good yields and excellent enantioselectivities. The method reported represents a valuable approach of utilizing β-ketoacids as synthetic equivalents of aryl/alkyl methyl ketone enolates.

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