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112913-64-1

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112913-64-1 Usage

Chemical Properties

White powder

Check Digit Verification of cas no

The CAS Registry Mumber 112913-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,1 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112913-64:
(8*1)+(7*1)+(6*2)+(5*9)+(4*1)+(3*3)+(2*6)+(1*4)=101
101 % 10 = 1
So 112913-64-1 is a valid CAS Registry Number.

112913-64-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name FMOC-MET-OSU

1.2 Other means of identification

Product number -
Other names Fmoc-L-methionine hydroxysuccinimide 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:112913-64-1 SDS

112913-64-1Downstream Products

112913-64-1Relevant articles and documents

Site-Specific Incorporation of Multiple Thioamide Substitutions into a Peptide Backbone via Solid Phase Peptide Synthesis

Yang, Jinhua,Wang, Changliu,Yao, Chaochao,Chen, Chunqiu,Hu, Yafang,He, Guifeng,Zhao, Junfeng

, p. 1484 - 1494 (2020/01/02)

Among various peptide modification strategies, thioamide substitution by replacing the carbonyl oxygen atom of an amide bond with a sulfur atom constitutes an invaluable tool for chemical biology, for use in peptide drug discovery and protein structure-fu

Acid-labile protecting groups for the synthesis of lipidated peptides

Kadereit, Dieter,Deck, Patrick,Heinemann, Ines,Waldmann, Herbert

, p. 1184 - 1193 (2007/10/03)

Lipidated peptides and their neolipoprotein derivatives are efficient tools for the investigation of biological processes in molecular detail. These compounds are often acid- and base-labile, and their synthesis requires the use of a combination of blocki

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