CC(=O)NCC1=CC=C(C=C1)C(=NC1=CC=C(C=C2NC(=O)NC2=O)C=C1)C1C(=O)NC2=C1C=C(C=C2)[N+]([O-])=O

InChIKey=ABUQAVFUVNBFCK-UHFFFAOYSA-N

C28H22N6O6

538.52

Organic compounds

Organoheterocyclic compounds

Azolidines

Imidazolidines

Imidazolidinones - Imidazolidinediones

Hydantoins

Alpha amino acids and derivatives Indolines 5-monosubstituted hydantoins Nitroaromatic compounds Ureides Benzene and substituted derivatives Secondary ketimines Acetamides Azomethines Dicarboximides Secondary carboxylic acid amides Lactams Organic oxoazanium compounds Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives Carbonyl compounds Organic salts Organic zwitterions Organopnictogen compounds Organic oxides

Aromatic heteropolycyclic compounds

Hydantoin - Alpha-amino acid or derivatives - Indole or derivatives - Dihydroindole - Nitroaromatic compound - 5-monosubstituted hydantoin - Ureide - Monocyclic benzene moiety - Benzenoid - Secondary ketimine - Azomethine - Acetamide - Dicarboximide - Lactam - Ketimine - Carboxamide group - Organic nitro compound - Urea - C-nitro compound - Secondary carboxylic acid amide - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic 1,3-dipolar compound - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Imine - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as hydantoins. These are heterocyclic compounds containing an imidazolidine substituted by ketone group at positions 2 and 4.

Not available