Compound Identification
SMILES
CC1=CC=CC=C1S(=O)(=O)NC1OC(=O)C(OC2=CC=CC=C2)=C1Br
InChIKey
InChIKey=HVMOYKLTZCGUQJ-UHFFFAOYSA-N
Formula
C17H14BrNO5S
Mass
424.27
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Benzenesulfonamides
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Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Benzenesulfonamides
Intermediate Tree Nodes
Not available
Direct Parent
Benzenesulfonamides
Alternative Parents
Benzenesulfonyl compounds Phenoxy compounds Toluenes Organosulfonamides Butenolides Vinylogous halides Aminosulfonyl compounds Enoate esters Lactones Vinyl bromides Oxacyclic compounds Bromoalkenes Monocarboxylic acids and derivatives Hydrocarbon derivatives Carbonyl compounds Organic oxides Organobromides Organonitrogen compounds Organopnictogen compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Benzenesulfonamide - Benzenesulfonyl group - Phenoxy compound - Toluene - 2-furanone - Organosulfonic acid amide - Dihydrofuran - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Vinylogous halide - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Aminosulfonyl compound - Carboxylic acid ester - Lactone - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Oxacycle - Bromoalkene - Haloalkene - Organoheterocyclic compound - Vinyl halide - Vinyl bromide - Organonitrogen compound - Organobromide - Organohalogen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Carbonyl group - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as benzenesulfonamides. These are organic compounds containing a sulfonamide group that is S-linked to a benzene ring.
External Descriptors
Not available