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2-Thiophenecarboxylic acid, 4-[4-(4-pyridinyl)phenyl]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

820224-07-5

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820224-07-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 820224-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,0,2,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 820224-07:
(8*8)+(7*2)+(6*0)+(5*2)+(4*2)+(3*4)+(2*0)+(1*7)=115
115 % 10 = 5
So 820224-07-5 is a valid CAS Registry Number.

820224-07-5SDS

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 methyl 4-(4-pyridin-4-ylphenyl)thiophene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Thiophenecarboxylic acid,4-[4-(4-pyridinyl)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:820224-07-5 SDS

820224-07-5Relevant academic research and scientific papers

Structure-based design and synthesis of novel non-zinc chelating MMP-12 inhibitors

Dublanchet, Anne-Claude,Ducrot, Pierre,Andrianjara, Charles,O'Gara, Margaret,Morales, Renaud,Compere, Delphine,Denis, Alexis,Blais, Stephane,Cluzeau, Philippe,Courte, Karine,Hamon, Jacques,Moreau, Francois,Prunet, Marie-Laure,Tertre, Anita

, p. 3787 - 3790 (2007/10/03)

A new class of MMP-12 inhibitors was discovered and optimized using structure-based drug design methods. Modeling studies using a known MMP-12 crystal structure identified a new interaction mode for these new MMP-12 inhibitors. Further optimization resulted in the discovery of a compound displaying nanomolar activity against MMP-12 and which was co-crystallized with MMP-12.

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