Structure Information
Structure

Compound Identification

SMILES

CC1=CC=C(S1)C(=O)CN1C(=O)N(C(=O)C1=O)C12CC3CC(CC(C3)C1)C2

InChIKey

InChIKey=CGPZXGULFMTYBR-UHFFFAOYSA-N

Formula

C20H22N2O4S

Mass

386.47

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Azolidines

Subclass

Imidazolidines

Intermediate Tree Nodes

Imidazolidinones - Imidazolidinediones

Direct Parent

Hydantoins

Alternative Parents

Alpha amino acids and derivatives Aryl alkyl ketones N-acyl ureas 2,5-disubstituted thiophenes Heteroaromatic compounds Dicarboximides Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - Aryl alkyl ketone - Aryl ketone - 2,5-disubstituted thiophene - Ureide - N-acyl urea - Heteroaromatic compound - Thiophene - Dicarboximide - Urea - Carbonic acid derivative - Ketone - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic heteropolycyclic compound

Description

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.

External Descriptors

Not available

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