Structure Information
Structure

Compound Identification

SMILES

COC1=C(C=C(C)C=C1)S(=O)(=O)N(CC(=O)NC1=C(C)C=CC(=C1)[N+]([O-])=O)C1=CC(Cl)=C(Cl)C=C1

InChIKey

InChIKey=RHNMMIHRFLJZJR-UHFFFAOYSA-N

Formula

C23H21Cl2N3O6S

Mass

538.4

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Benzenoids

Class

Benzene and substituted derivatives

Subclass

Sulfanilides

Intermediate Tree Nodes

Not available

Direct Parent

Sulfanilides

Alternative Parents

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

Sulfanilide - Benzenesulfonamide - Alpha-amino acid or derivatives - Anilide - Nitrotoluene - Nitrobenzene - Benzenesulfonyl group - Methoxybenzene - Phenoxy compound - 1,2-dichlorobenzene - N-arylamide - Phenol ether - Anisole - Nitroaromatic compound - Toluene - Alkyl aryl ether - Halobenzene - Chlorobenzene - Organosulfonic acid amide - Aryl halide - Aryl chloride - Aminosulfonyl compound - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Secondary carboxylic acid amide - C-nitro compound - Carboxamide group - Organic nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Ether - Organic oxoazanium - Hydrocarbon derivative - Organic zwitterion - Organic oxide - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Organic salt - Organochloride - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.

External Descriptors

Not available

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