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6-oxo-1,6-dihydropyridine-2,3-dicarboxylic acid is a chemical compound with the molecular formula C7H5NO4. It is a derivative of pyridine, a heterocyclic aromatic compound containing a nitrogen atom in a six-membered ring. This specific compound features a dihydropyridine structure, which means it has two hydrogen atoms added to the pyridine ring, and a 6-oxo group, indicating the presence of a carbonyl group at the 6th position. Additionally, it has two carboxylic acid groups attached to the 2nd and 3rd positions of the pyridine ring. 6-oxo-1,6-dihydropyridine-2,3-dicarboxylic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in the production of certain organic compounds.

7596-64-7

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7596-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7596-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7596-64:
(6*7)+(5*5)+(4*9)+(3*6)+(2*6)+(1*4)=137
137 % 10 = 7
So 7596-64-7 is a valid CAS Registry Number.

7596-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-oxo-1H-pyridine-2,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 6-Hydroxy-pyridin-2,3-dicarbonsaeure

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:7596-64-7 SDS

7596-64-7Downstream Products

7596-64-7Relevant academic research and scientific papers

Synthesis and spectral properties of 6(1H)-oxopyridine-2,3-dicarboxylic acid and metal porphyrazines based thereon

Galanin,Kudrik,Maizlish,Shaposhnikov

, p. 125 - 129 (2005)

Oxidation of quinolin-2-ol with potassium permanganate in alkaline medium gave 6(1H)-oxo-pyridine-2,3-dicarboxylic acid. The latter was reacted with urea in the presence of ammonium molybdate and bivalent metal chlorides to obtain the corresponding metal porphyrazines.

Oxidation of 2- and 3-Halogenated Quinolines: An Easy Access to 5- and 6-Halogenopyridine-2,3-dicarboxylic Acids

Bas, Marie-Delphine Le,Gueret, Caroline,Perrio, Cecile,Lasne, Marie-Claire,Barre, Louisa

, p. 2495 - 2499 (2007/10/03)

Pyridine-2,3-dicarboxylic acids bearing an halogen in the position α or β to the nitrogen atom were synthesized by oxidation of the corresponding quinolines. Two methods, using either ozone followed by hydrogen peroxide or ruthenium tetroxide under catalytic conditions were used. Diacids 1b,c and 2a-c substituted in 6-position by a chlorine or bromine and in 5-position by a fluorine, chlorine or bromine, respectively, were isolated in yields ranging from 46-71 percent. Yields of 6-fluoro and 6- or 5-iodo diacids 1a,d and 2d did not exceed 30 percent.

5 (and/or 6) substituted 2-(2-imidazolin-2-yl)nicotinic acids, esters and salts, useful as herbicidal agents and novel intermediates for the preparation of said nicotinic acids, esters and salts

-

, (2008/06/13)

There are provided novel 5(and/or 6)substituted 2-(2-imidazolin-2-yl) and 2-(2-imidazolidinyl)nicotinic acids, esters and salts, which are useful as herbicidal agents. There are also provided novel substituted pyrrolopyridine acetonitriles, pyrrolopyridin

CONTROLLED, REGIOSPECIFIC OXIDATION OF PYRIDINE CARBOXYLIC ACIDS AND ESTERS WITH ELEMENTAL FLUORINE

Puy, Michael Van Der,Nalewajek, David,Wicks, Gene E.

, p. 4389 - 4392 (2007/10/02)

Pyridine carboxylic acid salts or esters in water or water-acetonitrile mixtures were treated with elemental fluorine to give the corresponding 2-pyridones.

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