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876316-68-6

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876316-68-6 Usage

General Description

1-methyl-5-(thiophen-2-yl)-1H-pyrazole is a chemical compound with a molecular formula C9H9N3S. It is a pyrazole derivative with a methyl group and a thiophene ring attached to the 1- and 5- positions, respectively. 1-methyl-5-(thiophen-2-yl)-1H-pyrazole has potential applications in pharmaceutical research and development, particularly in the field of medicinal chemistry. It may exhibit biological activities and pharmacological properties that make it a target for drug discovery and design. Further studies and investigations into its chemical and biological properties could lead to potential therapeutic applications in the future.

Check Digit Verification of cas no

The CAS Registry Mumber 876316-68-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,3,1 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 876316-68:
(8*8)+(7*7)+(6*6)+(5*3)+(4*1)+(3*6)+(2*6)+(1*8)=206
206 % 10 = 6
So 876316-68-6 is a valid CAS Registry Number.

876316-68-6SDS

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 1-methyl-5-thiophen-2-ylpyrazole

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

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More Details:876316-68-6 SDS

876316-68-6Downstream Products

876316-68-6Relevant articles and documents

Indium-mediated synthesis of heterobiaryls

Font-Sanchis, Enrique,Cespedes-Guirao, F. Javier,Sastre-Santos, Angela,Fernandez-Lazaro, Fernando

, p. 3589 - 3591 (2008/02/04)

The palladium-mediated coupling reaction between triorganoindium reagents and organic electrophiles is extended to the synthesis of heteroaromatic compounds. Both electron-rich and electron-poor heterocycles can act as the organic electrophile or as the organoindium derivative.

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