[NH3+][C@@H](CO)C1=CC=CC=C1.[O-]C(=O)[C@H]1[C@@H]2OC[C@]3(NC(=O)NC3=O)[C@H]12

InChIKey=JDHRXLMROISHIU-UNZZUPCFSA-N

C16H19N3O6

349.343

Organic compounds

Organoheterocyclic compounds

Azolidines

Imidazolidines

Imidazolidinones - Imidazolidinediones

Hydantoins

Alpha amino acids and derivatives 5-monosubstituted hydantoins N-acyl ureas Aralkylamines Oxanes Cyclopropanecarboxylic acids Benzene and substituted derivatives Tetrahydrofurans Dicarboximides 1,2-aminoalcohols Oxacyclic compounds Monocarboxylic acids and derivatives Dialkyl ethers Carboxylic acids Azacyclic compounds Primary alcohols Organopnictogen compounds Organic salts Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds

Not available

Hydantoin - Alpha-amino acid or derivatives - 5-monosubstituted hydantoin - Aralkylamine - Ureide - N-acyl urea - Benzenoid - Oxane - Cyclopropanecarboxylic acid or derivatives - Cyclopropanecarboxylic acid - Monocyclic benzene moiety - Tetrahydrofuran - Dicarboximide - Urea - Carbonic acid derivative - 1,2-aminoalcohol - Oxacycle - Azacycle - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Primary amine - Primary alcohol - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Carbonyl group - Amine - Alcohol - 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