Structure Information
Structure

Compound Identification

SMILES

[Na+].CC(=O)NC1=C(I)C(C(N)=O)=C(I)C(C([O-])=O)=C1I

InChIKey

InChIKey=IBMNXUFJBIKZGC-UHFFFAOYSA-M

Formula

C10H6I3N2NaO4

Mass

621.871

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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 homomonocyclic compounds

Substituents

Acylaminobenzoic acid or derivatives - O-haloacetanilide - P-haloacetanilide - Haloacetanilide - Acetanilide - 2-halobenzoic acid or derivatives - 4-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - 2-halobenzoic acid - 4-halobenzoic acid - Halobenzoic acid - Benzamide - Benzoic acid - N-acetylarylamine - Anilide - N-arylamide - Benzoyl - 1-carboxy-2-haloaromatic compound - Halobenzene - Iodobenzene - Aryl iodide - Aryl halide - Vinylogous halide - Acetamide - Carboxamide group - Carboxylic acid salt - Primary carboxylic acid amide - Secondary carboxylic acid amide - Organic alkali metal salt - Carboxylic acid derivative - Carboxylic acid - Organic metal halide - Monocarboxylic acid or derivatives - Organic sodium salt - Organic oxide - Organic zwitterion - Organic salt - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic nitrogen compound - Organohalogen compound - Organoiodide - Organonitrogen compound - Organooxygen compound - Aromatic homomonocyclic 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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