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(CN3CCCC3)C=C2)C=C1

InChIKey

InChIKey=XQBOYJTYXDBBFQ-UHFFFAOYSA-N

Formula

C30H26N6O5

Mass

550.575

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