Structure Information
Structure

Compound Identification

SMILES

CCCCN1C(=O)NC(=O)\C1=C/C1=CN=C(CCCC)N1CC1=CC=C(NS(=O)(=O)C(F)(F)F)C=C1

InChIKey

InChIKey=YBEVDQXWKKPKBI-CPNJWEJPSA-N

Formula

C23H28F3N5O4S

Mass

527.56

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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 - Sulfanilide - 1,2,5-trisubstituted-imidazole - Trisubstituted imidazole - N-acyl urea - Ureide - N-substituted imidazole - Organic sulfonic acid amide - Organosulfonic acid amide - Monocyclic benzene moiety - Benzenoid - Organosulfonic acid or derivatives - Azole - Sulfonyl - Dicarboximide - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Imidazole - Heteroaromatic compound - Trihalomethane - Urea - Carbonic acid derivative - Carboxylic acid derivative - Azacycle - Organosulfur compound - Alkyl halide - Alkyl fluoride - Organopnictogen compound - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Organofluoride - Carbonyl group - Halomethane - Organic oxygen compound - Organic oxide - Organonitrogen compound - Organooxygen compound - 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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