Compound Identification
SMILES
CN(C1=C(C)C=C(Br)C=C1C(=O)NO)S(=O)(=O)C1=CC=C(OCC#C)C=C1
InChIKey
InChIKey=JMJKKHVSMQBPSU-UHFFFAOYSA-N
Formula
C18H17BrN2O5S
Mass
453.31
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
3-halobenzoic acids and derivatives Benzenesulfonamides m-Toluamides Benzenesulfonyl compounds Phenoxy compounds Phenol ethers Benzoyl derivatives Alkyl aryl ethers Bromobenzenes Organosulfonamides Aryl bromides Aminosulfonyl compounds Vinylogous amides Hydroxamic acids Acetylides Organic oxides Organobromides Organonitrogen compounds Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Sulfanilide - 3-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - Benzenesulfonamide - Benzoic acid or derivatives - Benzenesulfonyl group - M-toluamide - Toluamide - Benzoyl - Phenol ether - Phenoxy compound - Toluene - Halobenzene - Bromobenzene - Alkyl aryl ether - Organosulfonic acid amide - Aryl halide - Aryl bromide - Vinylogous amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Hydroxamic acid - Acetylide - Carboxylic acid derivative - Ether - Organooxygen compound - Organic oxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Organonitrogen compound - Organohalogen compound - Organobromide - 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