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(3RS,5S)-5-<2-(4-Bromophenyl)ethyl>-2-oxo-3-piperidinecarboxylic acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127633-49-2

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127633-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127633-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127633-49:
(8*1)+(7*2)+(6*7)+(5*6)+(4*3)+(3*3)+(2*4)+(1*9)=132
132 % 10 = 2
So 127633-49-2 is a valid CAS Registry Number.

127633-49-2Relevant articles and documents

Asymmetric synthesis of lometrexol ((6R)-5,10-dideaza-5,6,7,8-tetrahydrofolic acid)

Barnett,Wilson,Wendel,Winningham,Deeter

, p. 7038 - 7045 (2007/10/02)

An enantioselective synthesis of lometrexol (1) which utilizes (5R)-2-piperidone 18 as a key intermediate is described. Lipase-catalyzed enantioselective esterification of 1,3-propanediol derivative 5 provided (R)-(+)-6, the absolute configuration of whic

Enantioselective synthesis of antifolates

-

, (2008/06/13)

A process and intermediates for the enantioselective synthesis of 5,10-dideaza-5,6,7,8-tetrahydrofolic acid are disclosed.

Asymmetric synthesis and absolute configuration of 5,10-dideaza-5,6,7,8-tetrahydropteroic acid and 5,10-dideaza-5,6,7,8-tetrahydrofolic acid (DDATHF)

Barnett,Wilson

, p. 6291 - 6294 (2007/10/02)

Lipase-catalyzed enantioselective esterification of 2-substituted 1,3-diols has been utilized in the asymmetry synthesis and consequent configurational assignments of the title compounds.

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