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Butanoic acid, 2-hydroxy-3-(phenylmethoxy)-, ethyl ester, (2R,3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

524929-35-9

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524929-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 524929-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,4,9,2 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 524929-35:
(8*5)+(7*2)+(6*4)+(5*9)+(4*2)+(3*9)+(2*3)+(1*5)=169
169 % 10 = 9
So 524929-35-9 is a valid CAS Registry Number.

524929-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (2R,3S)-2-hydroxy-3-phenylmethoxybutanoate

1.2 Other means of identification

Product number -
Other names -

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:524929-35-9 SDS

524929-35-9Relevant academic research and scientific papers

A straight route towards glyceric chirons

Haddad, Mansour,Larcheveque, Marc

, p. 687 - 692 (2003)

Glycidic esters react with alcohols in the presence of a catalytic amount of magnesium perchlorate to give enantiopure 3-alkoxy-2-hydroxy esters regioselectively.

Diastereocontrolled synthesis of (-)-codonopsinine

Haddad, Mansour,Larchevêque, Marc

, p. 274 - 276 (2007/10/03)

An efficient process is described for the total synthesis of the alkaloid (-)-codonopsinine. The synthetic strategy is based on the diastereoselective hydrocyanation of a 2,3-dialkoxyaldehyde derived from L-threonine followed by a reductive alkylation of

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