Structure Information
Structure

Compound Identification

SMILES

CC(C)C1=CC=C(CCC(=O)NC2=CC=C(C=C2)S(=O)(=O)NC2=CC=C(Cl)C=C2)C=C1

InChIKey

InChIKey=KSHOSLOMLRFFQQ-UHFFFAOYSA-N

Formula

C24H25ClN2O3S

Mass

456.99

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Monoterpenoids

Intermediate Tree Nodes

Not available

Direct Parent

Aromatic monoterpenoids

Alternative Parents

Sulfanilides Monocyclic monoterpenoids Benzenesulfonamides Phenylpropanes Anilides Cumenes Benzenesulfonyl compounds N-arylamides Chlorobenzenes Organosulfonamides Aryl chlorides Fatty amides Aminosulfonyl compounds Secondary carboxylic acid amides Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides

Molecular Framework

Aromatic homomonocyclic compounds

Substituents

P-cymene - Aromatic monoterpenoid - Monocyclic monoterpenoid - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Anilide - Cumene - Phenylpropane - N-arylamide - Halobenzene - Chlorobenzene - Fatty amide - Aryl chloride - Aryl halide - Fatty acyl - Benzenoid - Monocyclic benzene moiety - Organosulfonic acid amide - Sulfonyl - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organochloride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organohalogen compound - Aromatic homomonocyclic compound

Description

This compound belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring.

External Descriptors

Not available

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