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9-Propyl-3,9-dihydro-6H-purin-6-one is a chemical compound belonging to the purine family, which is a heterocyclic aromatic organic compound consisting of a pyrimidine ring fused to an imidazole ring. This specific compound features a 9-propyl side chain attached to the purine core, and it is a dihydro derivative, meaning it has two hydrogen atoms added to the molecule, reducing its aromaticity. It is an important intermediate in the synthesis of various purine-based drugs and nucleosides, which have applications in the treatment of gout, cancer, and other diseases. The compound is also of interest in the field of medicinal chemistry due to its potential biological activities and its role in the development of new therapeutic agents.

6972-38-9

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6972-38-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6972-38-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6972-38:
(6*6)+(5*9)+(4*7)+(3*2)+(2*3)+(1*8)=129
129 % 10 = 9
So 6972-38-9 is a valid CAS Registry Number.

6972-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-n-Propylhypoxanthin

1.2 Other means of identification

Product number -
Other names 9-propyl-1,9-dihydro-purin-6-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:6972-38-9 SDS

6972-38-9Downstream Products

6972-38-9Relevant academic research and scientific papers

Ring-Centered Heterocyclic Cations and the Direct Heteroarylation of Aromatic and Heterocyclic Compounds

Song, Fenhong,St. Hilaire, Valentine R.,White, Emil H.

, p. 1957 - 1959 (2008/02/11)

(matrix presented) The protonation of heterocyclic diazotates (attachment adjacent to a nitrogen atom) yields ring-centered heterocyclic carbocations that are highly reactive. The carbocations were found to alkylate aromatic and heterocyclic compounds, such as benzene, N-methylpyrrole, and 2-aminopyridine, in reactions that are synthetically useful. This carbocation involvement may serve as a paradigm for the cross-linking of DNA by nitrous acid and the anticancer activity of heterocyclic diazotates.

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