Structure Information
Structure

Compound Identification

SMILES

Cl.[O-][N+](=O)C1=CC=C(CSCC2(CSCC3=CC=C(C=C3)[N+]([O-])=O)NC(=O)NC2=O)C=C1

InChIKey

InChIKey=ARNOSXMGMDYPFX-UHFFFAOYSA-N

Formula

C19H19ClN4O6S2

Mass

498.95

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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 - Alpha-amino acid or derivatives - Nitrobenzene - Nitroaromatic compound - 5-monosubstituted hydantoin - N-acyl urea - Ureide - Monocyclic benzene moiety - Benzenoid - Dicarboximide - C-nitro compound - Carbonic acid derivative - Urea - Organic nitro compound - Sulfenyl compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Thioether - Dialkylthioether - Carboxylic acid derivative - Azacycle - Organic oxoazanium - Hydrochloride - Organonitrogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen 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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