CC1CCC2=C(C=CC(F)=C2)N1C(=O)C1=C(Cl)C=C(C=C1)[N+]([O-])=O

InChIKey=QTFHMRGGUVFHSE-UHFFFAOYSA-N

C17H14ClFN2O3

348.76

Organic compounds

Organoheterocyclic compounds

Quinolines and derivatives

Hydroquinolines

Not available

Hydroquinolines

2-halobenzoic acids and derivatives Benzamides Nitrobenzenes Benzoyl derivatives Nitroaromatic compounds Chlorobenzenes Aryl chlorides Aryl fluorides Vinylogous halides Tertiary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organooxygen compounds Hydrocarbon derivatives Organic oxides Organic salts Organochlorides Organofluorides Organonitrogen compounds Organic cations

Aromatic heteropolycyclic compounds

Tetrahydroquinoline - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Nitrobenzene - Benzoic acid or derivatives - Benzamide - Benzoyl - Nitroaromatic compound - Chlorobenzene - Halobenzene - Benzenoid - Aryl fluoride - Monocyclic benzene moiety - Aryl chloride - Aryl halide - Vinylogous halide - Tertiary carboxylic acid amide - Organic nitro compound - C-nitro compound - Carboxamide group - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organic salt - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Organochloride - Organic cation - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as hydroquinolines. These are derivatives of quinoline in which in which at least one double bond in the quinoline moiety are reduced by adding two hydrogen atoms.

Not available