Structure Information
Structure

Compound Identification

SMILES

[Fe++].[Fe++].[CH]1[CH][CH][CH][CH]1.[CH]1[CH][CH][CH][CH]1.OC(=O)C1=C(O)C(NC(=O)CCC(C(=O)[C]2[CH][CH][CH][CH]2)C(=O)[C]2[CH][CH][CH][CH]2)=C(O)C=C1

InChIKey

InChIKey=HPDVSAGVHSBXNX-UHFFFAOYSA-N

Formula

C33H29Fe2NO7

Mass

663.283

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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

Not available

Substituents

Acylaminobenzoic acid or derivatives - Dihydroxybenzoic acid - Salicylic acid or derivatives - Salicylic acid - Hydroxybenzoic acid - Benzoic acid - Anilide - Benzoyl - N-arylamide - Resorcinol - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - 1,3-diketone - Phenol - Fatty amide - 1,3-dicarbonyl compound - Fatty acyl - Vinylogous acid - Secondary carboxylic acid amide - Ketone - Carboxamide group - Carboxylic acid derivative - Carboxylic acid - Cyclic olefin - Cycloalkene - Monocarboxylic acid or derivatives - Organic transition metal salt - Hydrocarbon derivative - Organic oxide - Unsaturated hydrocarbon - Unsaturated aliphatic hydrocarbon - Carbonyl group - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Olefin - Organonitrogen compound - Organooxygen compound - Hydrocarbon - Organic cation - 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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