Compound Identification
SMILES
CC(=O)C1=C(C)NC(SCC(=O)NC2=CC=C(Br)C=C2)=C(C#N)C1C1=CC=C(Cl)C=C1
InChIKey
InChIKey=XFHCYKXUBBJCGY-UHFFFAOYSA-N
Formula
C23H19BrClN3O2S
Mass
516.84
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 Bromobenzenes Chlorobenzenes Dihydropyridines Aryl bromides Aryl chlorides Vinylogous amides Secondary carboxylic acid amides Ketene acetals Ketones Sulfenyl compounds Azacyclic compounds Nitriles Hydrocarbon derivatives Organic oxides Organobromides Organochlorides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - N-arylamide - Bromobenzene - Chlorobenzene - Dihydropyridine - Halobenzene - Aryl bromide - Aryl chloride - Aryl halide - Hydropyridine - Vinylogous amide - Secondary carboxylic acid amide - Carboxamide group - Ketene acetal or derivatives - Ketone - Sulfenyl compound - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Nitrile - Carbonitrile - Organosulfur compound - Organohalogen compound - Organobromide - Organochloride - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organic oxide - Cyanide - Organic oxygen compound - Organic nitrogen 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