Compound Identification
SMILES
CC1=CC=CC(C)=C1NC(=O)C(C#N)=C1SC(CC2=CC(Cl)=CC=C2)C(=O)N1C1=CC=CC=C1
InChIKey
InChIKey=ZVIFZAKZKQVENH-UHFFFAOYSA-N
Formula
C27H22ClN3O2S
Mass
488.0
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
m-Xylenes N-arylamides Chlorobenzenes Vinylogous thioesters Aryl chlorides Vinylogous amides Thiazolidines Tertiary carboxylic acid amides Secondary carboxylic acid amides Ketene acetals Lactams Azacyclic compounds Nitriles Organic oxides Carbonyl compounds Hydrocarbon derivatives Organochlorides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - M-xylene - Xylene - N-arylamide - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Vinylogous thioester - Tertiary carboxylic acid amide - Thiazolidine - Vinylogous amide - Carboxamide group - Ketene acetal or derivatives - Lactam - Secondary carboxylic acid amide - Nitrile - Carbonitrile - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organic oxygen compound - Organic nitrogen compound - Organic oxide - Cyanide - Carbonyl group - Hydrocarbon derivative - 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