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Propanethioic acid, 2-[[(phenylmethoxy)carbonyl]amino]-, S-(phenylmethyl) ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

140668-74-2

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140668-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 140668-74-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,6,6 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 140668-74:
(8*1)+(7*4)+(6*0)+(5*6)+(4*6)+(3*8)+(2*7)+(1*4)=132
132 % 10 = 2
So 140668-74-2 is a valid CAS Registry Number.

140668-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-Benzyloxycarbonylamino-thiopropionic acid S-benzyl ester

1.2 Other means of identification

Product number -
Other names -

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:140668-74-2 SDS

140668-74-2Downstream Products

140668-74-2Relevant academic research and scientific papers

Facile peptide thioester synthesis via solution-phase tosylamide preparation

Manabe, Shino,Sugioka, Tomoyuki,Ito, Yukishige

, p. 849 - 853 (2007/10/03)

Preparation of peptide thioester is essential for native chemical ligation and block condensation. Our novel methodology involves conversion of the carboxylic acid of a peptide into a thioester using p-toluenesulfonyl isocyanate, followed by alkylation, t

Reverse proteolysis promoted by in situ generated peptide ester fragments

Wehofsky, Nicole,Koglin, Norman,Thust, Sven,Bordusa, Frank

, p. 6126 - 6133 (2007/10/03)

In this contribution we describe a general synthesis concept for the in situ preparation of protease specific reactants using methyl thioesters as universal precursors. The precursor esters are readily available by standard synthesis procedures and can be

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