Structure Information
Structure

Compound Identification

SMILES

OC1=C(C=C2NC(=O)N(CC3=CC=CC=C3F)C2=O)C=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=XLEBKQWWZYVUIE-UHFFFAOYSA-N

Formula

C17H12FN3O5

Mass

357.297

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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 heteromonocyclic compounds

Substituents

Hydantoin - Alpha-amino acid or derivatives - Nitrophenol - Nitrobenzene - Nitroaromatic compound - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Ureide - Fluorobenzene - N-acyl urea - Halobenzene - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Dicarboximide - Carbonic acid derivative - Urea - C-nitro compound - Organic nitro compound - 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 - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organooxygen compound - Organonitrogen compound - Organofluoride - Carbonyl group - Organohalogen compound - Aromatic 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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