Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=C(C=CC(Cl)=C1)C1=CC=C(O1)C1C2C(ON1C1=CC=CC=C1)C(=O)N(CC1=CC=CC=C1)C2=O

InChIKey

InChIKey=HKAFWWXDHNSTMU-UHFFFAOYSA-N

Formula

C28H20ClN3O6

Mass

529.93

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Azolidines

Subclass

Isoxazolidines

Intermediate Tree Nodes

Not available

Direct Parent

Phenylisoxazolidines

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phenylisoxazolidine - Nitrobenzene - N-phenylhydroxylamine - 1-hydroxylamino, 4-unsubstituted benzenoid - 1-hydroxylamino, 2-unsubstituted benzenoid - Nitroaromatic compound - Halobenzene - Chlorobenzene - 2-pyrrolidone - N-alkylpyrrolidine - Pyrrolidone - Benzenoid - Aryl chloride - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - Aryl halide - Pyrrolidine - Furan - Dicarboximide - Carboxylic acid imide - Heteroaromatic compound - Organic nitro compound - Lactam - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Oxacycle - Azacycle - N-organohydroxylamine - Organic 1,3-dipolar compound - Organic oxoazanium - Organic nitrogen compound - Organic zwitterion - Carbonyl group - Organic salt - Organic oxygen compound - Hydrocarbon derivative - Organohalogen compound - Organic oxide - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phenylisoxazolidines. These are heterocyclic compounds containing an isoxazolidine conjugated by a phenyl group.

External Descriptors

Not available

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