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5444-47-3

9-Phenyl-3,9-dihydro-1H-purine-2,6-dione is a chemical compound belonging to the purine family, characterized by a unique molecular structure. It is a derivative of the naturally occurring purine base, with a phenyl group attached at the 9th position and a dihydro functional group. 9-Phenyl-3,9-dihydro-1H-purine-2,6-dione is known for its potential applications in medicinal chemistry, particularly in the development of drugs targeting adenosine receptors, which play a crucial role in various physiological processes. The compound's structure allows for the modulation of these receptors, making it a subject of interest for researchers in the field of drug discovery and development.

5444-47-3

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5444-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5444-47-3 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 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5444-47:
(6*5)+(5*4)+(4*4)+(3*4)+(2*4)+(1*7)=93
93 % 10 = 3
So 5444-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N4O2/c16-10-8-9(13-11(17)14-10)15(6-12-8)7-4-2-1-3-5-7/h1-6H,(H2,13,14,16,17)

5444-47-3SDS

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 9-phenyl-3H-purine-2,6-dione

1.2 Other means of identification

Product number -
Other names 9-Phenyl-3,9-dihydro-purin-2,6-dion

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:5444-47-3 SDS

5444-47-3Relevant articles and documents

SYNTHESIS OF CROWN-CONTAINING XANTHINE DERIVATIVES

Ivanov, E. I.,Polishchuk, A. A.,Kalayanov, G. D.

, p. 1074 - 1078 (1992)

A number of new derivatives of xanthine, hypoxanthine, theophylline, and theobromine containing crown-ether substituents at the nitrogen atoms of the imidazole or pyrimidine nucleus was synthesized.

Selective adenosine reseptor compounds

-

, (2008/06/13)

Adenosine analogues which act selectively at adenosine receptors and which act in general as adenosine antagonists are disclosed. From in vitro studies it is known that specific physiological effects can be distinguished as a result of this selectivity an

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