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2-Oxazoleheptanoic acid, 5-phenyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

641636-83-1

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641636-83-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 641636-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,1,6,3 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 641636-83:
(8*6)+(7*4)+(6*1)+(5*6)+(4*3)+(3*6)+(2*8)+(1*3)=161
161 % 10 = 1
So 641636-83-1 is a valid CAS Registry Number.

641636-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 7-(5-phenyl-1,3-oxazol-2-yl)heptanoate

1.2 Other means of identification

Product number -
Other names 2-Oxazoleheptanoic acid,5-phenyl-,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:641636-83-1 SDS

641636-83-1Relevant academic research and scientific papers

COMPOUNDS, METHODS AND FORMULATIONS FOR THE ORAL DELIVERY OF A GLUCAGON LIKE PEPTIDE (GLP)-1 COMPOUND OR AN MELANOCORTIN 4 RECEPTOR (MC4) AGONIST PEPTIDE

-

Page/Page column 17, (2008/06/13)

The present invention relates to novel compounds, methods, and formulations useful for the oral delivery of a GLP-1 compound or an MC4 agonist peptide.

A novel series of histone deacetylase inhibitors incorporating hetero aromatic ring systems as connection units

Dai, Yujia,Guo, Yan,Curtin, Michael L.,Li, Junling,Pease, Lori J.,Guo, Jun,Marcotte, Patrick A.,Glaser, Keith B.,Davidsen, Steven K.,Michaelides, Michael R.

, p. 3817 - 3820 (2007/10/03)

A series of structurally novel HDAC inhibitors, in which a hetero aromatic ring connects the spacer with the hydrophobic group, has been designed and synthesized. These new inhibitors are very potent in in vitro enzymatic assays and display antiproliferation activity against two human cancer cell lines.

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