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Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC2=C(NC(=O)C2C(=NC2=CC=C(C=C3NC(=O)NC3=O)C=C2)C2=CC=C(CCN3CCCCC3=O)C=C2)C=C1

InChIKey

InChIKey=HLPUCPYUSONCTJ-UHFFFAOYSA-N

Formula

C32H28N6O6

Mass

592.612

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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 - Indole or derivatives - Dihydroindole - Nitroaromatic compound - 5-monosubstituted hydantoin - Piperidinone - Delta-lactam - Ureide - Piperidine - Monocyclic benzene moiety - Benzenoid - Azomethine - Secondary ketimine - Tertiary carboxylic acid amide - Dicarboximide - Urea - Carboxamide group - C-nitro compound - Secondary carboxylic acid amide - Organic nitro compound - Lactam - Ketimine - Carboxylic acid derivative - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic oxygen compound - Imine - Organic salt - Hydrocarbon derivative - Organic nitrogen compound - Organopnictogen compound - Carbonyl group - Organic zwitterion - Organooxygen compound - Organic oxide - Organonitrogen 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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