Compound Identification
SMILES
FC1=CC=CC=C1NS(=O)(=O)C1=CC=CC(NC(=O)CCCSC2=NC3=CC=CC=C3S2)=C1
InChIKey
InChIKey=BFJMRFGDWVDTRV-UHFFFAOYSA-N
Formula
C23H20FN3O3S3
Mass
501.61
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Sulfanilides
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Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Sulfanilides
Intermediate Tree Nodes
Not available
Direct Parent
Sulfanilides
Alternative Parents
Benzenesulfonamides Anilides Benzenesulfonyl compounds Benzothiazoles N-arylamides Alkylarylthioethers Fluorobenzenes Fatty amides Organosulfonamides Aryl fluorides Heteroaromatic compounds Aminosulfonyl compounds Thiazoles Secondary carboxylic acid amides Sulfenyl compounds Azacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organofluorides Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Benzenesulfonamide - Sulfanilide - 1,3-benzothiazole - Benzenesulfonyl group - Anilide - Aryl thioether - N-arylamide - Fluorobenzene - Halobenzene - Alkylarylthioether - Aryl fluoride - Aryl halide - Fatty amide - Organosulfonic acid amide - Fatty acyl - Thiazole - Sulfonyl - Azole - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Aminosulfonyl compound - Secondary carboxylic acid amide - Carboxamide group - Thioether - Organoheterocyclic compound - Azacycle - Sulfenyl compound - Carboxylic acid derivative - Organosulfur compound - Organic oxide - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organic oxygen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic 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