Compound Identification
SMILES
CSC1=CC=CC(NC(=O)C2CCC(CNS(=O)(=O)C3=CC=C(Br)S3)CC2)=C1
InChIKey
InChIKey=QWDSZBWRSPMMSA-UHFFFAOYSA-N
Formula
C19H23BrN2O3S3
Mass
503.49
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
Thiophenol ethers N-arylamides Alkylarylthioethers 2,5-disubstituted thiophenes Organosulfonamides Aryl bromides Heteroaromatic compounds Aminosulfonyl compounds Secondary carboxylic acid amides Sulfenyl compounds Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - Aryl thioether - Thiophenol ether - N-arylamide - 2,5-disubstituted thiophene - Alkylarylthioether - Aryl bromide - Aryl halide - Organosulfonic acid amide - Sulfonyl - Thiophene - Organic sulfonic acid or derivatives - Heteroaromatic compound - Organosulfonic acid or derivatives - Aminosulfonyl compound - Carboxamide group - Secondary carboxylic acid amide - Carboxylic acid derivative - Organoheterocyclic compound - Sulfenyl compound - Thioether - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - 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