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S-(2-oxo-2-phenylethyl)cysteine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83961-81-3

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83961-81-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83961-81-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,6 and 1 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83961-81:
(7*8)+(6*3)+(5*9)+(4*6)+(3*1)+(2*8)+(1*1)=163
163 % 10 = 3
So 83961-81-3 is a valid CAS Registry Number.

83961-81-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name S-Phenacyl-glutathion

1.2 Other means of identification

Product number -
Other names S-phenacyl-L-cysteine

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:83961-81-3 SDS

83961-81-3Relevant academic research and scientific papers

Efficient S-alkylation of cysteine in the presence of 1,1,3,3- tetramethylguanidine

W?ostowski, Marek,Czarnocka, Sylwia,MacIejewski, Piotr

experimental part, p. 5977 - 5979 (2010/11/21)

The synthesis of S-alkylated cysteine derivatives was carried out successfully in the presence of 1,1,3,3-tetramethylguanidine. Alkylation proceeded in high yields on unprotected amino acids and peptides containing a sulfhydryl group.

Novel N,S-phenacyl protecting group and its application for peptide synthesis

Tang, Guo,Ji, Tao,Hu, An-Fu,Zhao, Yu-Fen

scheme or table, p. 1907 - 1909 (2009/04/11)

The phenacyl group can be introduced onto amino and thio groups by N,S-alkylation reactions. Conversely, these groups are removed rapidly by employing magnesium in acetic acid. This protecting group was successfully applied to a short peptide synthesis of Boc-L-Cys-Gly-OMe. Georg Thieme Verlag Stuttgart.

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