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Glycine, N-(N-acetyl-L-alanyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82754-95-8

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82754-95-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82754-95-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,5 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 82754-95:
(7*8)+(6*2)+(5*7)+(4*5)+(3*4)+(2*9)+(1*5)=158
158 % 10 = 8
So 82754-95-8 is a valid CAS Registry Number.

82754-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-L-alanylglycine ethyl ester

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:82754-95-8 SDS

82754-95-8Downstream Products

82754-95-8Relevant academic research and scientific papers

Aqueous Solutions Containing Amino Acids and Peptides

Blackburn, G. Michael,Lilley, Terence H.,Walmsley, Elizabeth

, p. 1641 - 1666 (1982)

The energetics of the interactions occuring between some N-acetyl amino acid amides and some N-acetyl peptide amides in aqueous solutions at 298.15 K have been investigated.Osmotic coefficients of solutions containing N-acetylglycinamide (G), N-acetyl-L-a

KINETICS OF AMINOLYSIS FOR 1-THIO-β-D-GLUCOPYRANOSYL ESTERS OF N-ACYLALANINES

Horvat, S.,Tomic, S.,Jericevic, Z.

, p. 1047 - 1050 (2007/10/02)

The kinetics of aminolysis of 1-thio-β-D-glucopyranosyl esters of N-protected alanines (1) in dichloromethane at 26 deg C, by ethyl glycinate, under pseudo-first-order conditions follows the relationship kobsd=k2.Significant differences were obserwed in the rates of dipeptide forming aminolysis for 1-thiolesters 1a-1f, depending on N-acyl substituents and the configuration of alanine.

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