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N-(4-methylphenyl)-5H-purin-6-amine, also known as 4-methylphenyl-6-aminopurine, is an organic compound with the molecular formula C11H10N6. It is a derivative of purine, a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. This specific compound features a 4-methylphenyl group attached to the nitrogen atom at position 1 of the purine ring and an amino group at position 6. It is a white crystalline solid and is used as an intermediate in the synthesis of various purine-based compounds, including pharmaceuticals and agrochemicals. Due to its potential applications in drug development, it is an important compound in the field of medicinal chemistry.

5446-36-6

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5446-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5446-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5446-36:
(6*5)+(5*4)+(4*4)+(3*6)+(2*3)+(1*6)=96
96 % 10 = 6
So 5446-36-6 is a valid CAS Registry Number.

5446-36-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methylphenyl)-7H-purin-6-amine

1.2 Other means of identification

Product number -
Other names 6-p-Tolylaminopurine

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:5446-36-6 SDS

5446-36-6Relevant academic research and scientific papers

Microwave-assisted regioselective synthesis of acyclic nucleosides through an alkylating reaction with 2-oxa-1,4-butanediol diacetate

Qu, Guirong,Han, Suhui,Zhang, Zhiguang,Geng, Mingwei,Xue, Feng

, p. 819 - 824 (2007/10/03)

An efficient and green procedure for the synthesis of purine acyclic nucleosides through microwave-assisted, alkylation of various purine nucleobases with 2-oxa-1,4-butanediol diacetate in the absence of solvent and catalyst is described. The advantages of using this method include its environmental friendliness, simple manipulation, short reaction time, high regioselectivity, and good yields.

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