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36204-76-9

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36204-76-9 Usage

Description

3-Amino-N-methylpyrazine-2-carboxamide is an organic compound with the molecular formula C5H7N3O. It is a white crystalline solid and is known for its potential applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
3-Amino-N-methylpyrazine-2-carboxamide is used as a reactant in the synthesis of triazole derivatives that are known to inhibit eosinophilia. Eosinophilia is a condition characterized by an abnormally high number of eosinophils, a type of white blood cell, in the body. These triazole derivatives can be used as potential therapeutic agents for treating eosinophilia and related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 36204-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,0 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36204-76:
(7*3)+(6*6)+(5*2)+(4*0)+(3*4)+(2*7)+(1*6)=99
99 % 10 = 9
So 36204-76-9 is a valid CAS Registry Number.

36204-76-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-N-methylpyrazine-2-carboxamide

1.2 Other means of identification

Product number -
Other names 3-amino-N-methyl-2-pyrazinecarboxamide

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:36204-76-9 SDS

36204-76-9Downstream Products

36204-76-9Relevant articles and documents

INHIBITORS OF FOCAL ADHESION KINASE

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Page/Page column 132-133, (2008/12/07)

The invention provides inhibitors of focal adhesion kinase, an enzyme involved in the attachment of the cytoskeleton of a cell to an extracellular matrix, which has been implicated in processes such as cell migration, cell proliferation, and cell survival. The inhibitors are derivatives of a 5-substituted 2,4-diaminopyridine wherein the substituents are as defined herein. The invention also provides a method of using the inhibitors in treatment of cancer, and methods of preparation of the inhibitors by use of coupling reactions.

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