56162-63-1 Usage
Description
2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID, also known as 6-Phenyl-2,3-dihydro-2-oxo-3-pyridinecarboxylic acid, is a chemical compound that belongs to the class of pyridine carboxylic acids. It is a derivative of pyridine with a phenyl group attached to its structure. This unique structure and the presence of functional groups make it a valuable intermediate in the synthesis of various organic compounds and drug molecules.
Uses
Used in Pharmaceutical Industry:
2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and functional groups make it a valuable intermediate in the production of these compounds.
Used in Medicinal Chemistry:
2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID is used as a key intermediate in medicinal chemistry for the development of new drug molecules. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Drug Discovery Research:
2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID is used as a starting material in drug discovery research to explore its potential as a precursor for the development of new pharmaceuticals. Its unique structure and functional groups make it an attractive candidate for further investigation and development.
Check Digit Verification of cas no
The CAS Registry Mumber 56162-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,6 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56162-63:
(7*5)+(6*6)+(5*1)+(4*6)+(3*2)+(2*6)+(1*3)=121
121 % 10 = 1
So 56162-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO3/c14-11-9(12(15)16)6-7-10(13-11)8-4-2-1-3-5-8/h1-7H,(H,13,14)(H,15,16)
56162-63-1Relevant articles and documents
Rhodium-Catalyzed C4-Selective C-H Alkenylation of 2-Pyridones by Traceless Directing Group Strategy
Hazra, Sunit,Hirano, Koji,Miura, Masahiro
, p. 1388 - 1393 (2021/03/03)
A rhodium-catalyzed C4-selective C-H alkenylation of 3-carboxy-2-pyridones with styrenes has been developed. The carboxylic group at the C3 position works as the traceless directing group, and the corresponding C4-alkenylated 2-pyridones are obtained exclusively with concomitant decarboxylation. Unlike the reported procedures, the exclusive C4 selectivity is uniformly observed even in the presence of potentially more reactive C-H bonds at the C5 and C6 positions. By using this strategy, the multiply substituted 2-pyridone can be prepared via sequential C-H functionalization reactions.
Enaminones as building blocks in heterocyclic syntheses: Reinvestigating the product structures of enaminones with malononitrile. A novel route to 6-substituted-3-oxo-2,3-dihydropyridazine-4-carboxylic acids
Alnajjar, Abdul-Aziz,Abdelkhalik, Mervat Mohammed,Al-Enezi, Amal,Elnagdi, Mohamed Hilmy
experimental part, p. 68 - 77 (2009/08/15)
The reported structures of reaction products of enaminones with malononitrile in ethanolic piperidine are revised. A novel route to 2,3-dihydropyridazine-4-carboxylic acids 4a-c via reactions of 2-cyano-5-(dimethylamino)-5-arylpenta-2,4-dienamides 8a-c wi
Heterocyclic amides
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, (2008/06/13)
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