56162-63-1

Basic information

• Product Name: 2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID
• Synonyms: TIMTEC-BB SBB011312;CHEMBRDG-BB 4400282;LABOTEST-BB LT00246074;ASINEX-REAG BAS 05515865;2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID;AKOS BBS-00007045;VITAS-BB TBB013111;2-oxo-6-phenyl-1,2-dihydropyridine-3-carboxylic acid(SALTDATA: FREE)
• CAS NO: 56162-63-1
• Molecular Formula: C₁₂H₉NO₃
• Molecular Weight: 215.2
• Mol File: 56162-63-1.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 491.5°C at 760 mmHg
• Flash Point: 251°C
• Appearance: /
• Density: 1.362g/cm³
• Vapor Pressure: 1.78E-10mmHg at 25°C
• Refractive Index: 1.631
• CAS DataBase Reference: 2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID(56162-63-1)
• EPA Substance Registry System: 2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID(56162-63-1)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 56162-63-1(Hazardous Substances Data)

Usage

General Description

2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID is a chemical compound belonging to the class of pyridine carboxylic acids. It is also known as 6-Phenyl-2,3-dihydro-2-oxo-3-pyridinecarboxylic acid. 2-OXO-6-PHENYL-1,2-DIHYDRO-PYRIDINE-3-CARBOXYLIC ACID is a derivative of pyridine and has a phenyl group attached to its structure. It is used in the pharmaceutical industry as a building block for the synthesis of various organic compounds and drug molecules. Its unique structure and functional groups make it a valuable intermediate in the production of pharmaceuticals and agrochemicals. Additionally, it has potential applications in medicinal chemistry and drug discovery research.

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)

Upstream product

• 54818-68-7 2-cyano-5-dimethylamino-5-phenylpenta-2,4-dienoic acid amide 
• 888721-10-6 methyl 2-oxo-2H-[1,2'-bipyridine]-3-carboxylate 
• 125031-47-2 Methyl 1,2-Dihydro-2-oxo-6-phenyl-3-pyridinecarboxylate 
• 24959-22-6 (±)-2-benzoyl-3-phenylcyclopropane-1,1-dicarbonitrile 
• 43083-13-2 1,2-dihydro-2-oxo-6-phenylpyridine-3-carbonitrile 
• 104230-11-7 cis-1,1-dicyano-4-phenoxy-4-phenylbuta-1,3-diene 
• 104230-12-8 trans-1,1-dicyano-4-phenoxy-4-phenylbuta-1,3-diene 
• 43083-13-2 3-cyano-2-hydroxy-6-phenylpyridine 
• 4789-74-6 6-ethoxy-2-phenylquinoline 
• 393109-89-2 8-methoxy-2-phenylquinoline 
• 65288-80-4 2-amino-6-phenyl-nicotinic acid 
• 863770-87-0 2-phenylquinolin-6-amine 

Downstream Products

• 19006-82-7 2-hydroxy-6-phenylpyridine 
• 1045325-76-5 2-chloro-6-phenylisonicotinoyl chloride 
• 85815-02-7 1-methyl-2-oxo-6-phenyl-1,2-dihydropyridine-3-carboxylic acid 
• 147269-02-1 2-<3-<(benzyloxycarbonyl)amino>-2-oxo-6-phenyl-1,2-dihydro-1-pyridyl>-N-<2-<(tert-butyldimethylsilyl)oxy>-3,3,3-trifluoro-1-isopropylpropyl>acetamide 
• 147269-09-8 2-[3-benzyloxycarbonylamino-6-(4-methoxyphenyl)-2-oxo-1,2-dihydro-1-pyridyl]-N-(2-tert-butyldimethylsilyloxy-3,3,3-trifluoro-1-isopropylpropyl)acetamide 
• 1221899-03-1 C₂₀H₁₉N₃O₃ 
• 1159096-80-6 3-{[4-(1H-benzimidazol-2-yl)piperidin-1-yl]carbonyl}-6-phenylpyridin-2(1H)-one 
• 148638-71-5 (2-Methyl-4-oxo-7-phenyl-4H-pyrano[2,3-b]pyridin-3-yl)-phosphonic acid diethyl ester 
• 148638-69-1 [2-Oxo-2-(2-oxo-6-phenyl-1,2-dihydro-pyridin-3-yl)-ethyl]-phosphonic acid diethyl ester 
• 148638-68-0 3-(2-Methanesulfonyl-acetyl)-6-phenyl-1H-pyridin-2-one 

Relevant articles and documents

Base-catalysed 18F-labelling of trifluoromethyl ketones. Application to the synthesis of 18F-labelled neutrophil elastase inhibitors

A new method for the fluorine-18 labelling of trifluoromethyl ketones has been developed. This method is based on the conversion of a-COCF3 functional group to a difluoro enol silyl ether followed by halogenation and fluorine-18 labelling. The utility of this new method was demonstrated by the synthesis of fluorine-18 labelled neutrophil elastase inhibitors, which are potentially useful for detection of inflammatory disorders.

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

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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