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54950-12-8

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54950-12-8 Usage

Structure

Pyrimidine derivative with a pyridine ring attached to the 6th position of the pyrimidine ring

Functional Groups

Amino group ( \textNH2 ) at the 2nd position of the pyridine ring
Carbonyl group ( \textC=O ) at the 4th position of the pyrimidine ring

Common Use

Building block for synthesizing various drug molecules

Biological Activities

Studied for potential biological activities in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 54950-12-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,5 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54950-12:
(7*5)+(6*4)+(5*9)+(4*5)+(3*0)+(2*1)+(1*2)=128
128 % 10 = 8
So 54950-12-8 is a valid CAS Registry Number.

54950-12-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-pyridin-4-yl-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 2-amino-6-[4]pyridyl-3H-pyrimidin-4-one

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:54950-12-8 SDS

54950-12-8Downstream Products

54950-12-8Relevant articles and documents

HETEROARYLOXY-SUBSTITUTED PHENYLAMINOPYRIMIDINES AS RHO-KINASE INHIBITORS

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, (2010/02/06)

The invention relates to heteroaryloxy-substituted phenylaminopyrimidines, to methods for the production thereof, and to the use of the same for producing medicaments for the treatment and/or prophylaxis of diseases, especially cardiovascular diseases. The inventive compounds inhibit Rho-kinase.

RHO-KINASE INHIBITORS

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Page/Page column 11, (2008/06/13)

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PYRIMIDONE DERIVATIVES

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Page 56, (2008/06/13)

A pyrimidone derivative represented by the formula (I) or a salts thereof: wherein R1 represents an alkyl group, an alkenyl group, an alkynyl group, a cycloalkyl group, an aryl group and the like; R2 represents a hydrogen atom, hydro

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