CCCCCCCCCCCCOC(=O)C1=C(C[N+]2=CC=CC(=C2)C(N)=O)NC(C[N+]2=CC=CC(=C2)C(N)=O)=C(C1C1=CC=CC=C1)C(=O)OCCCCCCCCCCCC

InChIKey=HCRCUCAWEPUWEB-UHFFFAOYSA-P

C51H73N5O6

852.173

Organic compounds

Organoheterocyclic compounds

Pyridines and derivatives

Pyridinecarboxylic acids and derivatives

Pyridinecarboxamides - Nicotinamides

N-substituted nicotinamides

Dihydropyridines Pyridinium derivatives Benzene and substituted derivatives Dicarboxylic acids and derivatives Vinylogous amides Heteroaromatic compounds Enoate esters Primary carboxylic acid amides Amino acids and derivatives Azacyclic compounds Dialkylamines Enamines Carbonyl compounds Organic oxides Hydrocarbon derivatives Organic cations

Aromatic heteromonocyclic compounds

N-substituted nicotinamide - Dihydropyridine - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Hydropyridine - Benzenoid - Pyridinium - Heteroaromatic compound - Vinylogous amide - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - Primary carboxylic acid amide - Azacycle - Enamine - Secondary aliphatic amine - Carboxylic acid derivative - Secondary amine - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Carbonyl group - Organooxygen compound - Organic nitrogen compound - Organic cation - 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