Compound Identification
SMILES
CCCCC1=CC=C(C=C1)S(=O)(=O)C1=CN=C(NC1=O)SCC(=O)NC1=C(Br)C=C(C)C=C1
InChIKey
InChIKey=PJCOFDYOOMIFJV-UHFFFAOYSA-N
Formula
C23H24BrN3O4S2
Mass
550.49
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
- Subclass Anilides
-
Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Anilides
Intermediate Tree Nodes
Not available
Direct Parent
Anilides
Alternative Parents
Benzenesulfonyl compounds N-arylamides Alkylarylthioethers Toluenes Bromobenzenes Pyrimidones Hydropyrimidines Aryl bromides Sulfones Heteroaromatic compounds Lactams Secondary carboxylic acid amides Azacyclic compounds Sulfenyl compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organobromides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Benzenesulfonyl group - Anilide - Aryl thioether - N-arylamide - Bromobenzene - Halobenzene - Alkylarylthioether - Pyrimidone - Toluene - Aryl bromide - Aryl halide - Hydropyrimidine - Pyrimidine - Heteroaromatic compound - Sulfone - Sulfonyl - Carboxamide group - Lactam - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Sulfenyl compound - Thioether - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxide - Organic oxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
External Descriptors
Not available