Compound Identification
SMILES
[O-][N+](=O)C1=CC(=C(NN=CC2=C(F)C=CC=C2Cl)C=C1)S(=O)(=O)NC1=CC=CC=C1Cl
InChIKey
InChIKey=UOMDKBRFRQBWAV-UHFFFAOYSA-N
Formula
C19H13Cl2FN4O4S
Mass
483.3
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 Benzenesulfonyl compounds Nitrobenzenes Phenylhydrazines Nitroaromatic compounds Chlorobenzenes Fluorobenzenes Aryl chlorides Organosulfonamides Aryl fluorides Aminosulfonyl compounds Organic oxoazanium compounds Hydrazones Propargyl-type 1,3-dipolar organic compounds Organic oxides Organochlorides Organofluorides Hydrocarbon derivatives Organic salts Organic zwitterions
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Sulfanilide - Benzenesulfonamide - Nitrobenzene - Benzenesulfonyl group - Nitroaromatic compound - Phenylhydrazine - Halobenzene - Fluorobenzene - Chlorobenzene - Aryl halide - Aryl fluoride - Aryl chloride - Organosulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organic nitro compound - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Hydrazone - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organohalogen compound - Organic oxide - Organic nitrogen compound - Organic oxygen compound - Organic zwitterion - Organic salt - Hydrocarbon derivative - Organochloride - Organofluoride - Organonitrogen compound - Organosulfur compound - 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