Structure Information
Structure

Compound Identification

SMILES

[Na+].CC(C)C[C@H](C(CN1C(=O)C2=CC=CC=C2C1=O)C(=O)NO)C(=O)N[C@@H](CC1=CC=C(C=C1)S([O-])(=O)=O)C(=O)C1=CC=CO1

InChIKey

InChIKey=LPCVWSVFNWJXKZ-HFCHKYIYSA-M

Formula

C30H30N3NaO10S

Mass

647.63

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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 - Amphetamine or derivatives - Benzenesulfonate - Arylsulfonic acid or derivatives - Benzenesulfonyl group - 1-sulfo,2-unsubstituted aromatic compound - Isoindole - Aryl alkyl ketone - Aryl ketone - Monocyclic benzene moiety - Fatty amide - Benzenoid - N-acyl-amine - Fatty acyl - Carboxylic acid imide, n-substituted - Furan - Organic sulfonic acid or derivatives - Heteroaromatic compound - Carboxylic acid imide - Sulfonyl - Organosulfonic acid - Organosulfonic acid or derivatives - Carboxamide group - Hydroxamic acid - Ketone - Secondary carboxylic acid amide - Organic alkali metal salt - Azacycle - Oxacycle - Carboxylic acid derivative - Organonitrogen compound - Organic salt - Organic sodium salt - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organosulfur compound - Organic oxide - Organic cation - 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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