Structure Information
Structure

Compound Identification

SMILES

OCCN1C2CCCC1CC1(C2)NC(=O)NC1=O

InChIKey

InChIKey=KBAYASIIOBRTNU-UHFFFAOYSA-N

Formula

C12H19N3O3

Mass

253.302

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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

Azaspirodecane derivatives Alpha amino acids and derivatives 5-monosubstituted hydantoins N-acyl ureas Piperidines Dicarboximides Trialkylamines 1,2-aminoalcohols Azacyclic compounds Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Molecular Framework

Aliphatic heteropolycyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - Azaspirodecane - 5-monosubstituted hydantoin - N-acyl urea - Ureide - Piperidine - Dicarboximide - Urea - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carbonic acid derivative - 1,2-aminoalcohol - Azacycle - Alkanolamine - Carboxylic acid derivative - Hydrocarbon derivative - Organopnictogen compound - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxygen compound - Primary alcohol - Amine - Organic nitrogen compound - Alcohol - Organic oxide - Aliphatic heteropolycyclic 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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