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tert-butyl (S)-3-((R)-((tert-butoxycarbonyl)amino)(phenyl)methyl)-2-oxo-3-phenylindoline-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1043872-88-3

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1043872-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1043872-88-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,3,8,7 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1043872-88:
(9*1)+(8*0)+(7*4)+(6*3)+(5*8)+(4*7)+(3*2)+(2*8)+(1*8)=153
153 % 10 = 3
So 1043872-88-3 is a valid CAS Registry Number.

1043872-88-3Downstream Products

1043872-88-3Relevant academic research and scientific papers

Enantioselective direct Mannich reactions of 3-substituted oxindoles catalyzed by chiral phosphine via dual-reagent catalysis

Jin, Qiaowen,Zheng, Changwu,Zhao, Gang,Zou, Gang

, p. 4134 - 4144 (2018/06/25)

A combination of an amino acid-derived chiral phosphine catalyst and methyl acrylate to catalyze the direct Mannich reaction of 3-substituted oxindoles and imines has been reported to afford 3-tetrasubstituted oxindole derivatives which are key structures

Organocatalytic Stereoselective Mannich Reaction of 3-Substituted Oxindoles

Tian, Xu,Jiang, Kun,Peng, Jing,Du, Wei,Chen, Ying-Chun

supporting information; experimental part, p. 3583 - 3586 (2009/05/07)

(Chemical Equation Presented) The asymmetric Mannich reaction of 3-substituted oxindoles and N-Boc (mines was investigated for the first time, employing bifunctional thiourea-tertiary amine organocatalysts based on OPEN scaffold. The novel transformations

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