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Glycine, N-[(1,1-dioxido-1,2-thiazetidin-3-yl)acetyl]-L-phenylalanyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

757237-41-5

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757237-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 757237-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,7,2,3 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 757237-41:
(8*7)+(7*5)+(6*7)+(5*2)+(4*3)+(3*7)+(2*4)+(1*1)=185
185 % 10 = 5
So 757237-41-5 is a valid CAS Registry Number.

757237-41-5SDS

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-[(RS)-(1,1-dioxo-1,2-thiazetidin-3-yl)acetyl]-L-phenylalanylglycine methyl ester

1.2 Other means of identification

Product number -
Other names {(S)-2-[2-(1,1-Dioxo-1λ6-[1,2]thiazetidin-3-yl)-acetylamino]-3-phenyl-propionylamino}-acetic acid methyl 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:757237-41-5 SDS

757237-41-5Upstream product

757237-41-5Downstream Products

757237-41-5Relevant academic research and scientific papers

Substituted 1,2-thiazetidine 1,1-dioxides. Synthesis of (RS)- and (S)-1,2-thiazetidine-3-acetic acid 1,1-dioxide and its reactions with amino acids and dipeptides

Roehrich, Till,Thaher, Bassam Abu,Manicone, Nico,Otto, Hans-Hartwig

, p. 979 - 999 (2007/10/03)

(RS)-2-tert-Butyldimethylsilyl-1,2-thiazetidine-3-acetic acid 1,1-dioxide prepared from (RS)-5-benzyl-β-homocysteine was condensed via DCC/NHS with various L-amino acid esters or dipeptide esters yielding N-silylated β-sultam peptides. A β-sultam active e

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