CC1=C(C(C)=C(NN2CC(=CC=C2)C(N)=O)C=C1)[N+]([O-])=O

InChIKey=BSLMHKBGXDXSCS-UHFFFAOYSA-N

C14H16N4O3

288.307

Organic compounds

Organoheterocyclic compounds

Pyridines and derivatives

Pyridinecarboxylic acids and derivatives

Pyridinecarboxamides - Nicotinamides

N-substituted nicotinamides

Nitrotoluenes Nitrobenzenes m-Xylenes Phenylhydrazines Nitroaromatic compounds Dihydropyridines Primary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Alkylhydrazines Azacyclic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organic oxides Carbonyl compounds Organic salts Organic zwitterions

Aromatic heteromonocyclic compounds

N-substituted nicotinamide - Nitrotoluene - Nitrobenzene - Nitroaromatic compound - M-xylene - Xylene - Phenylhydrazine - Dihydropyridine - Monocyclic benzene moiety - Hydropyridine - Benzenoid - Carboxamide group - C-nitro compound - Organic nitro compound - Primary carboxylic acid amide - Carboxylic acid derivative - Alkylhydrazine - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic salt - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic zwitterion - Hydrazine derivative - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as n-substituted nicotinamides. These are nicotnamides in which the pyridine ring is substituted at position 1.

Not available