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(S)-3-hydroxy-4-cyanobutyric acid methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150966-86-2

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150966-86-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150966-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,9,6 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 150966-86:
(8*1)+(7*5)+(6*0)+(5*9)+(4*6)+(3*6)+(2*8)+(1*6)=152
152 % 10 = 2
So 150966-86-2 is a valid CAS Registry Number.

150966-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-methyl-(3-hydroxy-4-cyano)-butanoate

1.2 Other means of identification

Product number -
Other names methyl (S)-4-cyano-3-hydroxybutanoate

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:150966-86-2 SDS

150966-86-2Relevant academic research and scientific papers

Sequential kinetic resolution catalyzed by halohydrin dehalogenase

Elenkov, Maja Majeric,Tang, Lixia,Hauer, Bernhard,Janssen, Dick B.

, p. 4227 - 4229 (2007/10/03)

(Chemical Equation Presented) A sequential kinetic resolution catalyzed by halohydrin dehalogenase was employed for the synthesis of two valuable enantiopure building blocks. Resolution of methyl 4-chloro-3-hydroxybutanoate methylester ((R,S)-2) with use of a Trp249Phe mutant of halohydrin dehalogenase yielded methyl 4-cyano-3-hydroxybutanoate methylester ((S)-4) with 96.8% ee (40% yield) and (S)-2 with 95.2% ee (41% yield). This reaction is carried out in aqueous solution under mild conditions and provides access to a useful statin side-chain building block.

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