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72676-96-1

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72676-96-1 Usage

General Description

4-oxo-1,4-dihydro-3-pyridinecarboxylic acid, also known as alpha-ketohistidine, is a chemical compound with the molecular formula C6H5NO3. It is a derivative of histidine, an essential amino acid involved in various physiological processes in the human body. 4-oxo-1,4-dihydro-3-pyridinecarboxylic acid is formed through the oxidation of histidine and is a key intermediate in the biosynthesis of other important molecules such as carnosine, anserine, and other dipeptides. It has been studied for its potential role in oxidative stress and its antioxidant properties, making it of interest in the fields of biochemistry and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 72676-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,7 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 72676-96:
(7*7)+(6*2)+(5*6)+(4*7)+(3*6)+(2*9)+(1*6)=161
161 % 10 = 1
So 72676-96-1 is a valid CAS Registry Number.

72676-96-1SDS

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 4-oxo-1,4-dihydro-3-pyridinecarboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Pyridinecarboxylic acid,1,4-dihydro-4-oxo

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:72676-96-1 SDS

72676-96-1Relevant articles and documents

The Reaction of N -Trimethylsilyl-Substituted Heteroarylamines with Esters and Thioesters: An Efficient Protocol to Access Diheteroarylamides

Koperniku, Ana,Zamiri, Maryam,Grierson, David S.

, p. 1779 - 1790 (2019/04/05)

The S -benzyl thioester and methyl ester derivatives of a representative 4-pyridinone-based carboxylic acid were sufficiently activated to react efficiently in amide coupling reactions with the amide anion generated in situ from the N -trimethylsilyl derivative of different weakly nucleophilic heteroarylamines. In acetonitrile as solvent, the precipitated diheteroarylamide products were isolated in pure form by vacuum filtration. This simple amide bond forming protocol can be readily adapted to the parallel synthesis of compound libraries.

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