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17039-14-4

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17039-14-4 Usage

Structure

Contains a pyrimidine ring with a chlorophenyl group and two amino groups at the 2 and 4 positions

Uses

Building block in the synthesis of pharmaceuticals and agrochemicals, kinase inhibitor with potential anti-cancer and anti-inflammatory properties, research tool in studying protein kinases and cellular processes

Importance

Important intermediate in the synthesis of biologically active molecules and significant role in medicinal and chemical research

Check Digit Verification of cas no

The CAS Registry Mumber 17039-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,3 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17039-14:
(7*1)+(6*7)+(5*0)+(4*3)+(3*9)+(2*1)+(1*4)=94
94 % 10 = 4
So 17039-14-4 is a valid CAS Registry Number.

17039-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-chlorophenyl)pyrimidine-2,4-diamine

1.2 Other means of identification

Product number -
Other names 5-(4-chloro-phenyl)-pyrimidine-2,4-diyldiamine

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:17039-14-4 SDS

17039-14-4Relevant articles and documents

Mechanochemical Magnesium-Mediated Minisci C-H Alkylation of Pyrimidines with Alkyl Bromides and Chlorides

Wu, Chongyang,Ying, Tao,Yang, Xinjie,Su, Weike,Dushkin, Alexandr V.,Yu, Jingbo

, p. 6423 - 6428 (2021)

A novel method to synthesize 4-alkylpyrimidines by the mechanochemical magnesium-mediated Minisci reaction of pyrimidine derivatives and alkyl halides has been reported. The reaction process operates with a broad substrate scope and excellent regioselectivity under mild conditions with no requirement of transition-metal catalysts, solvents, and inert gas protection. The practicality of this protocol has been demonstrated by the up-scale synthesis, mechanochemical product derivatization, and antimalarial drug pyrimethamine preparation.

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