Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC=C(C=C1)C(=O)COC(=O)C1=CC=CC=C1N1C(=O)C2CC(Br)C(Br)CC2C1=O

InChIKey

InChIKey=UMLJLPQWOXLQOM-UHFFFAOYSA-N

Formula

C23H18Br2N2O7

Mass

594.212

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Benzenoids

Class

Benzene and substituted derivatives

Subclass

Benzoic acids and derivatives

Intermediate Tree Nodes

Not available

Direct Parent

Acylaminobenzoic acid and derivatives

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Acylaminobenzoic acid or derivatives - Alkyl-phenylketone - 1-phenylpyrrolidine - Benzoate ester - Isoindolone - Isoindoline - Isoindole - Isoindole or derivatives - Phenylketone - Nitrobenzene - Benzoyl - Nitroaromatic compound - Aryl ketone - Aryl alkyl ketone - Carboxylic acid imide, n-substituted - Pyrrolidone - 2-pyrrolidone - Carboxylic acid imide - Dicarboximide - Pyrrole - Pyrrolidine - Organic nitro compound - Carboxylic acid ester - C-nitro compound - Lactam - Ketone - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organic oxoazanium - Organoheterocyclic compound - Azacycle - Organic 1,3-dipolar compound - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Organic salt - Organohalogen compound - Organobromide - Organonitrogen compound - Carbonyl group - Alkyl bromide - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as acylaminobenzoic acid and derivatives. These are derivatives of amino benzoic acid derivatives where the amine group is N-acylated.

External Descriptors

Not available

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