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L-Alanine, N-[N-[(1,1-dimethylethoxy)carbonyl]-3-[(phenylmethyl)dithio]-L-alanyl]-, (4-nitrophenyl)methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114518-92-2

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114518-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114518-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,1 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114518-92:
(8*1)+(7*1)+(6*4)+(5*5)+(4*1)+(3*8)+(2*9)+(1*2)=112
112 % 10 = 2
So 114518-92-2 is a valid CAS Registry Number.

114518-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-4-nitrobenzyl 2-((R)-3-(benzyldisulfanyl)-2-((tert-butoxycarbonyl)amino)propanamido)propanoate

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:114518-92-2 SDS

114518-92-2Downstream Products

114518-92-2Relevant academic research and scientific papers

PEPTIDE SYNTHESIS BY PRIOR THIOL CAPTURE-V. THE SCOPE AND CONTROL OF DISULFIDE INTERCHANGE DURING THE ACYL TRANSFER STEP

Kemp, D.S.,Fotouhi, Nader

, p. 4637 - 4640 (1987)

Disulfide interchange in DMSO, during amide formation by prior thiol capture is reduced to less than 3percent at low concentrations (10 M) of substrate in the absence of air and light, and in the presence of 2.5 to 10 mole percent AgNO3.The rate and sele

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