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2-MERCAPTO-3,6-DIPHENYL-3H-THIENO[2,3-D]PYRIMIDIN-4-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

315710-78-2

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315710-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 315710-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,5,7,1 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 315710-78:
(8*3)+(7*1)+(6*5)+(5*7)+(4*1)+(3*0)+(2*7)+(1*8)=122
122 % 10 = 2
So 315710-78-2 is a valid CAS Registry Number.

315710-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-mercapto-3,6-diphenyl-3H-thieno[2,3-d]pyrimidin-4-one

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:315710-78-2 SDS

315710-78-2Relevant academic research and scientific papers

SUBSTITUED 3,4-DIHYDROTHIENO [2,3-D] PYRMIDINES AS TISSUE TRANSGLUTAMINASE INHIBITORS

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Page/Page column 57; 66-67, (2010/11/08)

The present invention provides novel compounds and methods useful for treating transglutaminase associated disorders such as celiac spru, Alzheimer's disease and Huntington's disease. Certain compounds of the invention are tissue transglutaminase inhibito

Structure-activity relationship study of novel tissue transglutaminase inhibitors

Duval, Eric,Case, April,Stein, Ross L.,Cuny, Gregory D.

, p. 1885 - 1889 (2007/10/03)

Thieno[2,3-d]pyrimidin-4-one acylhydrazide derivatives were discovered as moderately potent inhibitors of TGase 2 (tissue transglutaminase) utilizing a fluorescence-based assay that measured TGase 2 catalyzed incorporation of the dansylated Lys derivative

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