Structure Information
Structure

Compound Identification

SMILES

CC(=O)NC1=CC=C(C=C1)C(=O)OCCOC(=O)C1[C@@H](C2=CC=CC=C2[N+]([O-])=O)C(C(=O)OC[C@@H]2CCCO2)=C(C)N=C1C

InChIKey

InChIKey=ZCZLJRKASXVMKV-XRQMUJOTSA-N

Formula

C31H33N3O10

Mass

607.616

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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 heteromonocyclic compounds

Substituents

Acylaminobenzoic acid or derivatives - Acetanilide - Benzoate ester - N-acetylarylamine - Dihydropyridinecarboxylic acid derivative - Nitrobenzene - Anilide - Nitroaromatic compound - Benzoyl - N-arylamide - Dihydropyridine - Dicarboxylic acid or derivatives - Hydropyridine - Acetamide - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Oxolane - Organic nitro compound - Carboxamide group - Carboxylic acid ester - Ketimine - C-nitro compound - Secondary carboxylic acid amide - Organoheterocyclic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Dialkyl ether - Propargyl-type 1,3-dipolar organic compound - Ether - Allyl-type 1,3-dipolar organic compound - Azacycle - Oxacycle - Organic oxoazanium - Hydrocarbon derivative - Organic nitrogen compound - Organic salt - Imine - Organic zwitterion - Organic oxygen compound - Organic oxide - Carbonyl group - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic 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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