Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(CC2=CN(CC3=CC=C(O)C=C3)C(\N=C\C3NC(=O)NC3=O)=N2)C=C1

InChIKey

InChIKey=DOYWIXSPFQRXOY-FOKLQQMPSA-N

Formula

C22H21N5O4

Mass

419.441

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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 - 1,2,4-trisubstituted-imidazole - Anisole - Phenoxy compound - Phenol ether - Trisubstituted imidazole - 5-monosubstituted hydantoin - Methoxybenzene - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - N-acyl urea - Phenol - Ureide - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Heteroaromatic compound - Azole - Dicarboximide - Imidazole - Shiff base - Urea - Carbonic acid derivative - Aldimine - Azacycle - Carboxylic acid derivative - Ether - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carbonyl group - Organooxygen compound - Organopnictogen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Organic oxygen compound - Imine - Organic nitrogen 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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