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4-Hydroxy-6-Methyl-1,5-Naphthyridine-3-carboxylic acid is a chemical compound with the molecular formula C10H8N2O3. It is a derivative of 1,5-naphthyridine, a heterocyclic compound consisting of a fused pyridine and pyridazine ring system. The molecule features a hydroxyl group at the 4-position, a methyl group at the 6-position, and a carboxylic acid group at the 3-position. 4-hydroxy-6-Methyl-1,5-Naphthyridine-3-carboxylic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs. Its unique structure and functional groups make it an interesting target for chemical modifications and exploration of its properties in different chemical contexts.

5000-82-8

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5000-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5000-82-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5000-82:
(6*5)+(5*0)+(4*0)+(3*0)+(2*8)+(1*2)=48
48 % 10 = 8
So 5000-82-8 is a valid CAS Registry Number.

5000-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-6-methyl-[1,5]naphthyridine-3-carboxylic acid

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:5000-82-8 SDS

5000-82-8Relevant academic research and scientific papers

Substituted 1,5-naphthyridine azolinones

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Page/Page column 9; 19, (2010/11/24)

Substituted 1,5-naphthyridine azolinones inhibit Cdk1 and are selective against Cdk2 and Cdk4. These compounds and their pharmaceutically acceptable salts have antiproliferative activity and are useful as anti-cancer agents.

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