Structure Information
Structure

Compound Identification

SMILES

NCCCC1=CC=C(C=C1)C(=NC1=CC=C(C=C2NC(=O)NC2=O)C=C1)C1C(=O)NC2=C1C=C(C=C2)[N+]([O-])=O

InChIKey

InChIKey=OEMUBXMSFWONBO-UHFFFAOYSA-N

Formula

C28H24N6O5

Mass

524.537

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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 heteropolycyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - Phenylpropylamine - Dihydroindole - Indole or derivatives - Nitroaromatic compound - 5-monosubstituted hydantoin - Ureide - Aralkylamine - Benzenoid - Monocyclic benzene moiety - Azomethine - Dicarboximide - Secondary ketimine - Ketimine - C-nitro compound - Amino acid or derivatives - Secondary carboxylic acid amide - Lactam - Urea - Carboxamide group - Organic nitro compound - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Azacycle - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organopnictogen compound - Primary aliphatic amine - Organonitrogen compound - Organooxygen compound - Imine - Organic nitrogen compound - Amine - Primary amine - Organic zwitterion - Carbonyl group - Organic salt - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aromatic 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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