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5817-96-9

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5817-96-9 Usage

General Description

6H-Pyrrolo[2,3-d]pyrimidin-6-one, 5,7-dihydro- (8CI) is a chemical compound with the molecular formula C6H6N2O. It is a heterocyclic compound that contains a pyrrolopyrimidine core structure. 6H-Pyrrolo[2,3-d]pyrimidin-6-one, 5,7-dihydro- (8CI) is a dihydro derivative of pyrrolopyrimidinone, with a double bond between carbon atoms 5 and 7. It may have potential applications in pharmaceuticals, as heterocyclic compounds are often used as building blocks for drug development. Additionally, this compound may exhibit biological activity and could be of interest for further research in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 5817-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,1 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5817-96:
(6*5)+(5*8)+(4*1)+(3*7)+(2*9)+(1*6)=119
119 % 10 = 9
So 5817-96-9 is a valid CAS Registry Number.

5817-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-dihydropyrrolo[2,3-d]pyrimidin-6-one

1.2 Other means of identification

Product number -
Other names -

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:5817-96-9 SDS

5817-96-9Downstream Products

5817-96-9Relevant articles and documents

Convenient synthesis of 2-substituted 5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-ones

Kókai, Eszter,Nagy, József,Tóth, Tünde,Kupai, József,Huszthy, Péter,Simig, Gyula,Volk, Balázs

, p. 767 - 773 (2016/03/23)

A new synthetic route was elaborated at our laboratory providing a convenient access to 5,7-dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-ones (diazaoxindoles), a compound family of biological relevance. Treatment of the easily available ethyl 2-(4-chloropyrimidin-5-yl)acetate derivatives with ammonia afforded the corresponding 2-(4-aminopyrimidin-5-yl)acetamides, which were finally cyclized to the target compounds.

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