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28944-98-1

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28944-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28944-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,9,4 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28944-98:
(7*2)+(6*8)+(5*9)+(4*4)+(3*4)+(2*9)+(1*8)=161
161 % 10 = 1
So 28944-98-1 is a valid CAS Registry Number.

28944-98-1SDS

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 Z-L-Ala-L-Trp-OMe

1.2 Other means of identification

Product number -
Other names (S)-2-((S)-2-Benzyloxycarbonylamino-propionylamino)-3-(1H-indol-3-yl)-propionic 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:28944-98-1 SDS

28944-98-1Relevant articles and documents

Metal-free direct amidation of peptidyl thiol esters with α-amino acid esters

Chen, Hao,He, Maomao,Wang, Yaya,Zhai, Linhui,Cui, Yongbo,Li, Yangyan,Lee, Yan,Zhou, Haibing,Hong, Xuechuan,Deng, Zixin

, p. 2723 - 2726 (2011/11/06)

Metal-free direct amidation of peptidyl thiol esters with α-amino acid esters in the presence of bis(trimethylsilyl) acetamide (BSA) has been developed. This general method provides convenient access to N-protected peptides in good yields under mild condi

Dehydrogenation of Indolines to Indoles via Azasulphonium Salts or N-Chloramines

Kawase, Masami,Miyake, Yuko,Kikugawa, Yasuo

, p. 1401 - 1404 (2007/10/02)

The dehydrogenation of indolines to indoles without using mineral oxidising reagents is described.The conversion was achieved via either azasulphonium salts or N-chloramines, the former route involving milder conditions but a more complex procedure.

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