Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=NNS(=O)(=O)C2=CC=C(C=C3NC(=O)NC3=O)C=C2)C=C1

InChIKey

InChIKey=DAUAXAKXSKTQFO-UHFFFAOYSA-N

Formula

C18H16N4O5S

Mass

400.41

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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

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Hydantoin - Benzenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonyl group - Phenoxy compound - Methoxybenzene - 5-monosubstituted hydantoin - Phenol ether - Anisole - Ureide - N-acyl urea - Alkyl aryl ether - Benzenoid - Hydrazinosulfonyl compound - Sulfonohydrazide - Monocyclic benzene moiety - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Dicarboximide - Urea - Carbonic acid derivative - Azacycle - Ether - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic heteromonocyclic 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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