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D-Alanine, N-[N-[(phenylmethoxy)carbonyl]glycyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24955-56-4

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24955-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24955-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,5 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24955-56:
(7*2)+(6*4)+(5*9)+(4*5)+(3*5)+(2*5)+(1*6)=134
134 % 10 = 4
So 24955-56-4 is a valid CAS Registry Number.

24955-56-4SDS

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 Z-Gly-D-Ala-OMe

1.2 Other means of identification

Product number -
Other names Z-Gly-D-AlaOMe

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:24955-56-4 SDS

24955-56-4Relevant academic research and scientific papers

Papain Catalysed Peptide Synthesis: Control of Amidase Activity and the Introduction of Unusual Amino Acids

Barbas, Carlos F. III,Wong, Chi-Huey

, p. 533 - 534 (2007/10/02)

Procedures for the papain catalysed synthesis of peptides containing D-amino acids and derivatives with control of the enzyme's amidase activity have been developed.

2(1H)-Pyridone as Leaving Group in Acylation Reactions - Applications in Peptide Synthesis

Effenberger, Franz,Brodt, Werner

, p. 468 - 482 (2007/10/02)

Alkyl 2-pyridyl carbonates 3 or mixtures of 3 and the isomeric N-(alkoxycarbonyl)-2-pyridones 3' are useful for the introduction of urethane protective groups into amino acids.The N-protected amino acids 7 - 10 react with 2(1H)-pyridone (1a) using the carbodiimide method to yield 2-pyridyl active esters 11, which easily undergo coupling reactions with amino acid esters 12 with elimination of 1a to give peptides 13 in good yields as well as high optical purities.

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