Structure Information
Structure

Compound Identification

SMILES

ClC1=CC=C(C=C1)N1C(=O)C2CC(CCN2C1=O)NC(=O)C1=CC=NC=C1

InChIKey

InChIKey=ULLBABBMTMYCTN-UHFFFAOYSA-N

Formula

C19H17ClN4O3

Mass

384.82

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Azolidines

Subclass

Imidazolidines

Intermediate Tree Nodes

Imidazolidinones - Imidazolidinediones - Hydantoins

Direct Parent

Phenylhydantoins

Alternative Parents

Phenylimidazolidines Alpha amino acids and derivatives Pyridinecarboxamides Chlorobenzenes N-acyl ureas Aryl chlorides Piperidines Heteroaromatic compounds Dicarboximides Secondary carboxylic acid amides Azacyclic compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Organopnictogen compounds

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

3-phenylhydantoin - Phenylimidazolidine - Alpha-amino acid or derivatives - Pyridinecarboxamide - Pyridine carboxylic acid or derivatives - Chlorobenzene - Halobenzene - N-acyl urea - Ureide - Aryl halide - Benzenoid - Pyridine - Monocyclic benzene moiety - Piperidine - Aryl chloride - Heteroaromatic compound - Dicarboximide - Urea - Secondary carboxylic acid amide - Carboxamide group - Carbonic acid derivative - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phenylhydantoins. These are heterocyclic aromatic compounds containing an imiazolidinedione moiety substituted by a phenyl group.

External Descriptors

Not available

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