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82679-58-1

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82679-58-1 Usage

General Description

D-Threonine benzyl ester is a chemical compound derived from threonine, an essential amino acid. It is created through the esterification of threonine with benzyl alcohol. D-THREONINE BENZYL ESTER is commonly used in the synthesis of peptides and proteins, particularly in the pharmaceutical industry. It is also utilized in the development of new drugs and as a biochemical research reagent, due to its ability to modify the structure and properties of proteins. Additionally, D-threonine benzyl ester has been studied for its potential therapeutic applications in the treatment of various diseases and disorders, making it a valuable chemical in the field of medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 82679-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,7 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82679-58:
(7*8)+(6*2)+(5*6)+(4*7)+(3*9)+(2*5)+(1*8)=171
171 % 10 = 1
So 82679-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO3/c1-8(13)10(12)11(14)15-7-9-5-3-2-4-6-9/h2-6,8,10,13H,7,12H2,1H3/t8-,10+/m0/s1

82679-58-1SDS

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 benzyl (2R,3S)-2-amino-3-hydroxybutanoate

1.2 Other means of identification

Product number -
Other names H-D-Thr-OBzl

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:82679-58-1 SDS

82679-58-1Relevant articles and documents

Stereoselective synthesis of natural and non-natural thomsen-nouveau antigens and hydrazide derivatives

Shaik, Ahmad Ali,Nishat, Sharmeen,Andreana, Peter R.

, p. 2582 - 2585 (2015/06/16)

A selective glycosylation strategy enabling access to all stereochemical combinations of tumor associated Thomsen-nouveau (Tn) antigen, d-GalNAc-O-Ser/Thr, has been developed. The key component for selectivity is the phthalimide-protected d- or l-amino acid acceptors which allow access to α- or β-anomers in excellent yields (72-96%) and selectivity (~100%) when appropriate C-2 substitution is installed. The glycoamino acid intermediates were divergently converted to Tn-based carboxylates or to hydrazides by tandem Pd-C debenzylation followed by treatment with hydrazine hydrate or hydrazine hydrate treatment alone.

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