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Glycine, N-L-alanyl-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66880-74-8

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66880-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66880-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,8 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66880-74:
(7*6)+(6*6)+(5*8)+(4*8)+(3*0)+(2*7)+(1*4)=168
168 % 10 = 8
So 66880-74-8 is a valid CAS Registry Number.

66880-74-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Alanylglycine tert-butyl ester

1.2 Other means of identification

Product number -
Other names ((S)-2-Amino-propionylamino)-acetic acid tert-butyl 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:66880-74-8 SDS

66880-74-8Upstream product

66880-74-8Downstream Products

66880-74-8Relevant academic research and scientific papers

The tetrabenzylglucosyloxycarbonyl(BGloc)-group-A carbohydrate-derived enzyme-labile urethane protecting group

Kappes, Thomas,Waldmann, Herbert

, p. 341 - 349 (1997)

The development of the tetrabenzylglucosyloxycarbonyl (BGloc)- protecting group as an enzymatically removable urethane protecting function for peptide synthesis is described. BGloc-protected amino acids are readily synthesized by conversion of amino acid allyl esters into the respective isocyanates, subsequent treatment with 2,3,4,6-tetrabenzylglucose and C- terminal allyl ester cleavage. From BGloc masked dipeptide esters, which are accessible by standard methods of peptide chemistry, the N-terminal urethane is selectively cleaved off in high yield via removal of the benzyl ethers by hydrogenation followed by hydrolysis of the urethane by means of α- and β- glucosidase under very mild reaction conditions.

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