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(S)-2-amino-2-(2-phenyl-1H-indol-3-yl)acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1427282-75-4

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1427282-75-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427282-75-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,2,8 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1427282-75:
(9*1)+(8*4)+(7*2)+(6*7)+(5*2)+(4*8)+(3*2)+(2*7)+(1*5)=164
164 % 10 = 4
So 1427282-75-4 is a valid CAS Registry Number.

1427282-75-4Upstream product

1427282-75-4Downstream Products

1427282-75-4Relevant academic research and scientific papers

Highly diastereoselective synthesis of 3-indolylglycines via an asymmetric oxidative heterocoupling reaction of a chiral nickel(ii) complex and indoles

Lin, Daizong,Wang, Jiang,Zhang, Xu,Zhou, Shengbin,Lian, Jie,Jiang, Hualiang,Liu, Hong

, p. 2575 - 2577 (2013)

The asymmetric synthesis of 3-indolylglycine derivatives was achieved by an oxidative heterocoupling reaction. This method for the selective C-3 functionalization of unprotected indoles with the chiral equivalent of a nucleophilic glycine nickel(ii) complex afforded adducts with high diastereoselectivities. The decomposition of adducts readily afforded 3-indolylglycine derivatives in high yields.

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