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(R)-3-(1-naphthoyl)-4-((R)-(3-bromophenyl)(hydroxy)methyl)-2,2,4-trimethyloxazolidin-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1539291-91-2

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1539291-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1539291-91-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,3,9,2,9 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1539291-91:
(9*1)+(8*5)+(7*3)+(6*9)+(5*2)+(4*9)+(3*1)+(2*9)+(1*1)=192
192 % 10 = 2
So 1539291-91-2 is a valid CAS Registry Number.

1539291-91-2Relevant academic research and scientific papers

Substrate control in enantioselective and diastereoselective aldol reaction by memory of chirality: A rapid access to enantiopure β-hydroxy quaternary α-amino acids

Viswambharan, Baby,Gori, Didier,Guillot, Regis,Kouklovsky, Cyrille,Alezra, Valerie

supporting information, p. 788 - 791 (2014/03/21)

An asymmetric aldol reaction by memory of chirality is reported with a substrate control of stereoselectivity by aldehyde and rationalized. Starting from l-alanine, several diastereopure and enantioenriched β-hydroxy quaternary α-amino acids have been obtained in three steps. The initial chirality of l-alanine is memorized through the dynamic axial chirality of tertiary aromatic amide.

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