CC1(C)CC(C)(C2=CC=C(Cl)C=C2)C2=CC=CC=C2N1C(=O)C1=C(Cl)C=CC(=C1)[N+]([O-])=O

InChIKey=FJLRRZKJYPCOBE-UHFFFAOYSA-N

C25H22Cl2N2O3

469.36

Organic compounds

Organoheterocyclic compounds

Quinolines and derivatives

Phenylquinolines

Not available

Phenylquinolines

2-halobenzoic acids and derivatives Hydroquinolines Benzamides Nitrobenzenes Benzoyl derivatives Nitroaromatic compounds Chlorobenzenes Aryl chlorides 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 Organonitrogen compounds Organic cations

Aromatic heteropolycyclic compounds

Phenylquinoline - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Tetrahydroquinoline - Nitrobenzene - Benzamide - Benzoic acid or derivatives - Nitroaromatic compound - Benzoyl - Halobenzene - Chlorobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Vinylogous halide - Tertiary carboxylic acid amide - C-nitro compound - Organic nitro compound - Carboxamide group - Azacycle - Organic 1,3-dipolar compound - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - 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 - Organohalogen compound - Organochloride - Organic cation - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as phenylquinolines. These are heterocyclic compounds containing a quinoline moiety substituted with a phenyl group.

Not available