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7H-Pyrano[2,3-d]pyrimidin-7-one (9CI) is a heterocyclic compound belonging to the pyrano[2,3-d]pyrimidine family. It features a pyrimidine ring fused to a pyran ring, with a carbonyl group at the 7-position. 7H-Pyrano[2,3-d]pyrimidin-7-one (9CI) is of interest in medicinal chemistry and drug design due to its potential biological activities and its ability to form the core structure of various pharmaceuticals. The 7H-Pyrano[2,3-d]pyrimidin-7-one scaffold can be further modified to create derivatives with specific therapeutic properties, making it a versatile building block in the development of new drugs.

4425-51-8

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4425-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4425-51-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,2 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4425-51:
(6*4)+(5*4)+(4*2)+(3*5)+(2*5)+(1*1)=78
78 % 10 = 8
So 4425-51-8 is a valid CAS Registry Number.

4425-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrano[2,3-d]pyrimidin-7-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:4425-51-8 SDS

4425-51-8Upstream product

4425-51-8Downstream Products

4425-51-8Relevant academic research and scientific papers

158. Reaktionen des Cumalinsaeure-methylesters und Cumalinaldehyds mit ambidenten Nucleophilen

Kvita, Vratislav,Sauter, Hanspeter,Tuck, Brian

, p. 1467 - 1473 (1988)

Reactions of Methyl Coumalate and Coumalaldehyde with Ambident Nucleophiles Methyl coumalate and coumalaldehyde show great diversity in their reactions with ambident nucleophiles both depending upon the 2H-pyran-2-one derivative and the nature of the ambi

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