CC1=CC=C(C=C1)C1=NC2=C(C)C=C(Br)C=C2C(=C1)C(=O)NC1=CC=C(C=C1)[N+]([O-])=O

InChIKey=QNKNRXHAYAKWBO-UHFFFAOYSA-N

C24H18BrN3O3

476.33

Organic compounds

Organoheterocyclic compounds

Quinolines and derivatives

Phenylquinolines

Not available

Phenylquinolines

Aromatic anilides Quinoline carboxamides Phenylpyridines Haloquinolines Pyridinecarboxylic acids and derivatives Nitrobenzenes Nitroaromatic compounds Toluenes Aryl bromides Heteroaromatic compounds Secondary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organic oxides Hydrocarbon derivatives Organic salts Organic zwitterions Organobromides Organonitrogen compounds Organooxygen compounds

Aromatic heteropolycyclic compounds

Phenylquinoline - Aromatic anilide - Quinoline-4-carboxamide - 2-phenylpyridine - Haloquinoline - Pyridine carboxylic acid or derivatives - Nitrobenzene - Nitroaromatic compound - Toluene - Aryl bromide - Aryl halide - Pyridine - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organobromide - Organic oxygen compound - Organohalogen compound - Organic salt - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - 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