Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=C(C)NC(CC)=C(C1C1=C(OCCCCN2C(=O)C3=CC=CC=C3C2=O)C=CC(=C1)[N+]([O-])=O)C(=O)OCC

InChIKey

InChIKey=WKADUEPEEMUPBY-UHFFFAOYSA-N

Formula

C32H35N3O9

Mass

605.644

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Isoindoles and derivatives

Subclass

Isoindolines

Intermediate Tree Nodes

Isoindolones

Direct Parent

Phthalimides

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Phthalimide - Nitrophenyl ether - Dihydropyridinecarboxylic acid derivative - Isoindole - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Alkyl aryl ether - Dihydropyridine - Monocyclic benzene moiety - Dicarboxylic acid or derivatives - Hydropyridine - Carboxylic acid imide, n-substituted - Benzenoid - Carboxylic acid imide - Vinylogous amide - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Amino acid or derivatives - Carboxylic acid ester - Organic nitro compound - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Secondary amine - Carboxylic acid derivative - Propargyl-type 1,3-dipolar organic compound - Secondary aliphatic amine - Azacycle - Enamine - Ether - Organic 1,3-dipolar compound - Organic oxoazanium - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic zwitterion - Organooxygen compound - Amine - Organic salt - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as phthalimides. These are aromatic heterocyclic compounds containing a 1,3-dioxoisoindoline moiety. They are imide derivatives of phthalic anhydrides.

External Descriptors

Not available

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