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1492-23-5

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1492-23-5 Usage

Definition

ChEBI: The O-succinyl derivative of L-homoserine.

Check Digit Verification of cas no

The CAS Registry Mumber 1492-23-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1492-23:
(6*1)+(5*4)+(4*9)+(3*2)+(2*2)+(1*3)=75
75 % 10 = 5
So 1492-23-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO6/c9-5(8(13)14)3-4-15-7(12)2-1-6(10)11/h5H,1-4,9H2,(H,10,11)(H,13,14)/t5-/m0/s1

1492-23-5SDS

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 O-succinyl-L-homoserine

1.2 Other means of identification

Product number -
Other names (2S)-2-amino-4-(3-carboxypropanoyloxy)butanoic acid

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:1492-23-5 SDS

1492-23-5Upstream product

1492-23-5Relevant articles and documents

Comparison of the sustainability metrics of the petrochemical and biomass-based routes to methionine

Sanders, Johan P.M.,Sheldon, Roger A.

, p. 44 - 49 (2015/01/16)

Sustainability metrics, based on material efficiency, energy input, land use and costs, of three processesfor the manufacture of methionine are compared. The petrochemical process affords dl-methionine whilethe two biomass-based routes afford the l-enantiomer. From the point of view of the major application,in animal feed, either can be used. The first bio-based route, developed by CJ Cheil-Jedang, involves theproduction of an l-methionine precursor, O-succinyl homoserine by fermentation followed by enzymaticreaction of the latter with methyl mercaptan.The second bio-based route involves the isolation of l-methionine from grass protein. Based on thisconcise evaluation of the sustainability metrics we conclude that both bio-based processe are potentiallyattractive sustainable routes for the manufacture of methionine.

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