CC1=CC(=C(C=C1)C1=CC=C(O1)\C=C(/C#N)C(=O)NC1=CC=CC=C1C(O)=O)[N+]([O-])=O

InChIKey=QOPKMCXGZPIICG-SDNWHVSQSA-N

C22H15N3O6

417.377

Organic compounds

Benzenoids

Benzene and substituted derivatives

Benzoic acids and derivatives

Not available

Acylaminobenzoic acid and derivatives

Anilides Benzoic acids Nitrobenzenes Nitrotoluenes Benzoyl derivatives N-arylamides Nitroaromatic compounds Vinylogous amides Furans Heteroaromatic compounds Secondary carboxylic acid amides Nitriles Oxacyclic compounds Propargyl-type 1,3-dipolar organic compounds Carboxylic acids Organic oxoazanium compounds Organic zwitterions Hydrocarbon derivatives Carbonyl compounds Organic salts Organic oxides

Aromatic heteromonocyclic compounds

Acylaminobenzoic acid or derivatives - Benzoic acid - Nitrobenzene - Nitrotoluene - Anilide - Nitroaromatic compound - Benzoyl - N-arylamide - Toluene - Furan - Heteroaromatic compound - Vinylogous amide - Carboxamide group - C-nitro compound - Organic nitro compound - Secondary carboxylic acid amide - Carboxylic acid derivative - Carboxylic acid - Carbonitrile - Nitrile - Oxacycle - Organic oxoazanium - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Cyanide - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic salt - Organic oxide - Organic zwitterion - Organic oxygen compound - Carbonyl group - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.

Not available