Structure Information
Structure

Compound Identification

SMILES

CC1=CC(Cl)=C(C=C1)N1N=NN=C1SCC(=O)NC1=C(C=C(C=C1)C(N)=O)[N+]([O-])=O

InChIKey

InChIKey=JDRVRMZIZUCBIS-UHFFFAOYSA-N

Formula

C17H14ClN7O4S

Mass

447.85

Export to:

JSON SDF CSV

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 - Phenyltetrazole - Nitrobenzene - Anilide - Benzamide - N-arylamide - Aryl thioether - Nitroaromatic compound - Benzoyl - Chlorobenzene - Halobenzene - Toluene - Alkylarylthioether - Aryl chloride - Aryl halide - Tetrazole - Heteroaromatic compound - Azole - Carboxamide group - Organic nitro compound - C-nitro compound - Primary carboxylic acid amide - Secondary carboxylic acid amide - Sulfenyl compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Thioether - Propargyl-type 1,3-dipolar organic compound - Azacycle - Carboxylic acid derivative - Organic oxoazanium - Organoheterocyclic compound - Organic zwitterion - Organic salt - Organic oxygen compound - Organohalogen compound - Organic nitrogen compound - Organochloride - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - 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

Previous Back Next