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"4(1H)-Pyrimidinone, 2,6-diamino-5-phenyl-" is a chemical compound with the molecular formula C11H11N5O. It is a derivative of pyrimidinone, featuring two amino groups at the 2nd and 6th positions, and a phenyl group at the 5th position. 4(1H)-Pyrimidinone, 2,6-diamino-5-phenyl- is known for its potential applications in pharmaceuticals and as an intermediate in the synthesis of various biologically active molecules. Its structure provides a foundation for further chemical modifications, making it a valuable component in the development of new drugs and therapeutic agents.

3415-83-6

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3415-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3415-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,1 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3415-83:
(6*3)+(5*4)+(4*1)+(3*5)+(2*8)+(1*3)=76
76 % 10 = 6
So 3415-83-6 is a valid CAS Registry Number.

3415-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-diamino-5-phenyl-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names 5-Phenyl-2,4-diamino-6-pyrimidinol

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:3415-83-6 SDS

3415-83-6Relevant academic research and scientific papers

5-Substituted-2,4-diamino-6-[2-(phosphonomethoxy) ethoxy]pyrimidines-Acyclic Nucleoside Phosphonate Analogues with Antiviral Activity

Hocková, Dana,Holy, Antonín,Masojídková, Milena,Andrei, Graciela,Snoeck, Robert,De Clercq, Erik,Balzarini, Jan

, p. 5064 - 5073 (2007/10/03)

2,4-Diamino-6-hydroxypyrimidines substituted in position 5 by an allyl, benzyl, cyanomethyl, ethoxycarbonylmethyl, phenyl, cyclopropyl, or methyl group were prepared either by C5-alkylation or by formation of the pyrimidine ring by cyclization. Their alky

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