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4-methylglutamic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14561-55-8

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14561-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14561-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,6 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14561-55:
(7*1)+(6*4)+(5*5)+(4*6)+(3*1)+(2*5)+(1*5)=98
98 % 10 = 8
So 14561-55-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO4/c1-3(5(8)9)2-4(7)6(10)11/h3-4H,2,7H2,1H3,(H,8,9)(H,10,11)/t3-,4+/m1/s1

14561-55-8SDS

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 (2S)-2-amino-4-methylpentanedioic acid

1.2 Other means of identification

Product number -
Other names DL-erythro-4-fluoroglutamic 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:14561-55-8 SDS

14561-55-8Relevant academic research and scientific papers

SYNTHESIS OF ω-HYDROXY ANALOGUES OF VALINE, LEUCINE AND ISOLEUCINE

Englisch-Peters, Sabine

, p. 6127 - 6134 (2007/10/02)

The isomers of γ-hydroxy-valine (6) were prepared by a modified Erlenmeyer synthesis and the δ-hydroxy analogues each of leucine (16a) and isoleucine (16b) were synthesized via 1,4-Michael addition.The diastereomers of 6 could be separated by column chrom

FLAME-INDUCED CARBOXYLATION OF UNSATURATED AMINES IN AN AQUEOUS FORMIC ACID SOLUTION

Nomoto, Shinya,Harada, Kaoru

, p. 145 - 148 (2007/10/02)

When a hydrogen-oxygen flame was kept in contact with an aqueous formic acid solution of unsaturated amines, carboxylation onto a double bond took place.This reaction revealed to be initiated by addition of a hydrogen atom to the double bond followed by coupling of the resulted substrate radical with a carboxyl radical.

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