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862828-08-8

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862828-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862828-08-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,8,2 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 862828-08:
(8*8)+(7*6)+(6*2)+(5*8)+(4*2)+(3*8)+(2*0)+(1*8)=198
198 % 10 = 8
So 862828-08-8 is a valid CAS Registry Number.

862828-08-8SDS

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 (4S)-3-[(2S)-6-bromo-2-methylhexanoyl]-4-(phenylmethyl)-1,3-oxazolidin-2-one

1.2 Other means of identification

Product number -
Other names 3(2S),(4S)-3-(2-methyl-6-bromo-1-oxohexanyl)-4-(phenylmethyl)-2-oxazolidinone

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:862828-08-8 SDS

862828-08-8Downstream Products

862828-08-8Relevant articles and documents

NON-NATURAL AMINO ACIDS AND NEUROTENSIN ANALOGUES THEREOF

-

Page/Page column 74, (2010/11/27)

This invention relates to non-natural desamino amino acid compounds, methods of making, and peptides containing these compounds as their N-terminus moieties. A preferred example is neurotensin (8-13) in which the N terminus is an alpha desamino N,N dimeth

Asymmetric synthesis of ω-bromo-2(S)-methyl acids as precursors for novel arginine, lysine, and mercapto residues

Hadden, M. Kyle,Kokko, Kyle P.,Dix, Thomas A.

, p. 1675 - 1680 (2007/10/03)

A series of ω-bromo-2(S)-methyl acids has been synthesized as precursors of novel arginine (Arg), lysine (Lys), and mercapto analogues. These intermediates contain α-methyl groups and are designed to mask the N-terminal amine when incorporated in pharmaceutically relevant peptides. Copyright Taylor & Francis, Inc.

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