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Glycine, 2-(acetyloxy)-N-[N-[(phenylmethoxy)carbonyl]-L-alanyl]-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89625-84-3

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89625-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89625-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,6,2 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89625-84:
(7*8)+(6*9)+(5*6)+(4*2)+(3*5)+(2*8)+(1*4)=183
183 % 10 = 3
So 89625-84-3 is a valid CAS Registry Number.

89625-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-carbobenzyloxy-L-alanyl-D,L-2-acetoxyglycine benzyl ester

1.2 Other means of identification

Product number -
Other names N-Carbobenzoxy-L-alanyl-D,L-2-acetoxyglycine benzyl ester

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:89625-84-3 SDS

89625-84-3Relevant academic research and scientific papers

Syntheses of 5′-Nucleoside Monophosphate Derivatives with Unique Aminal, Hemiaminal, and Hemithioaminal Functionalities: A New Class of 5′-Peptidyl Nucleotides

De, Swarup,Groaz, Elisabetta,Margamuljana, Lia,Herdewijn, Piet

, p. 8167 - 8180 (2016/06/15)

A number of synthetically useful transformations have been developed to generate novel 5′-peptidyl nucleoside monophosphate analogues that incorporate sensitive phosphoaminal, -hemiaminal or -hemithioaminal functionalities. The strategies adopted entailed

A Novel Peptide Delivery System Involving Peptidase Activated Prodrugs as Antimicrobial Agents. Synthesis and Biological Activity of Peptidyl Derivatives of 5-Fluorouracil

Kingsbury, William D.,Boehm, Jeffrey C.,Mehta, Rajanikant J.,Grappel, Sarah F.,Gilvarg, Charles

, p. 1447 - 1451 (2007/10/02)

As an approach to the development of antimicrobial agents, a novel peptide carrier system was designed, based on the chemical instability of α-substituted glycine analogues, with the explicit intent of actively transporting therapeutically useful compound

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