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(3R)-5-oxo-3-Pyrrolidineacetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

808157-06-4

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808157-06-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 808157-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,8,1,5 and 7 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 808157-06:
(8*8)+(7*0)+(6*8)+(5*1)+(4*5)+(3*7)+(2*0)+(1*6)=164
164 % 10 = 4
So 808157-06-4 is a valid CAS Registry Number.

808157-06-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-(+)-2-oxo-4-pyrrolidineacetic acid

1.2 Other means of identification

Product number -
Other names (4R)-4-carboxymethyl-pyrrolidin-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:808157-06-4 SDS

808157-06-4Relevant academic research and scientific papers

MANUFACTURING PROCESS FOR (S)-PREGABALIN

-

Page/Page column 14-15, (2012/05/20)

The present invention relates to a novel manufacturing process and novel intermediates useful in the synthesis of pharmaceutically active compounds of general formula (I) used for treatment of epilepsy, neuropathic pain, anxiety and social phobia. The invention describes preparation of enantiomerically pure (S)-Pregabalin from chiral pyrrolidin-2-one of formula (IV).

A convenient chemoenzymatic synthesis of (R)-(-) and (S)-(+)-homo-β- proline

Felluga, Fulvia,Gombac, Valentina,Pitacco, Giuliana,Valentin, Ennio

, p. 3323 - 3327 (2007/10/03)

Both enantiomers of the heterocyclic GABA analogue homo-β-proline (3-pyrrolidineacetic acid) were synthesized by a chemoenzymatic method involving the use of two enantiocomplementary enzymes in the disymmetric hydrolyses of 3-nitromethylglutaric acid diethyl ester.

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