Structure Information
Structure

Compound Identification

SMILES

O=C1NC(=O)C(N1)=C1CCOC1=O

InChIKey

InChIKey=MBAHDQHEBHYEAF-UHFFFAOYSA-N

Formula

C7H6N2O4

Mass

182.135

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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 5-monosubstituted hydantoins N-acyl ureas Gamma butyrolactones Vinylogous amides Tetrahydrofurans Dicarboximides Enoate esters Oxacyclic compounds Azacyclic compounds Monocarboxylic acids and derivatives Organonitrogen compounds Carbonyl compounds Organic oxides Organopnictogen compounds Hydrocarbon derivatives

Molecular Framework

Aliphatic heteromonocyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - 5-monosubstituted hydantoin - N-acyl urea - Ureide - Gamma butyrolactone - Dicarboximide - Tetrahydrofuran - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous amide - Carboxylic acid ester - Urea - Lactone - Carbonic acid derivative - Azacycle - Carboxylic acid derivative - Oxacycle - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organooxygen compound - Organonitrogen compound - Aliphatic 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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