Compound Identification
SMILES
CC1=C(Br)C=CC(NC(=O)CSC2=NC(=CS2)C2=CC=C(Cl)C=C2)=C1
InChIKey
InChIKey=UITINZWJCYUQEF-UHFFFAOYSA-N
Formula
C18H14BrClN2OS2
Mass
453.8
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
N-arylamides Toluenes 2,4-disubstituted thiazoles Alkylarylthioethers Bromobenzenes Chlorobenzenes Aryl bromides Aryl chlorides Heteroaromatic compounds Secondary carboxylic acid amides Sulfenyl compounds Azacyclic compounds Organochlorides Organic oxides Organobromides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - N-arylamide - Aryl thioether - Halobenzene - Chlorobenzene - Toluene - 2,4-disubstituted 1,3-thiazole - Alkylarylthioether - Bromobenzene - Aryl bromide - Aryl halide - Aryl chloride - Thiazole - Azole - Heteroaromatic compound - Secondary carboxylic acid amide - Carboxamide group - Azacycle - Organoheterocyclic compound - Sulfenyl compound - Carboxylic acid derivative - Thioether - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organohalogen compound - Organobromide - Organochloride - Organonitrogen compound - Organooxygen 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