Compound Identification
SMILES
CC1=CC(OCC2=NN=C(SCC(=O)NC3=CC(Cl)=CC(Cl)=C3)N2CC=C)=C(C)C=C1
InChIKey
InChIKey=VOLMSGSNHJRQEO-UHFFFAOYSA-N
Formula
C22H22Cl2N4O2S
Mass
477.4
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
Dichlorobenzenes N-arylamides Phenol ethers Phenoxy compounds p-Xylenes Alkylarylthioethers Alkyl aryl ethers Aryl chlorides Heteroaromatic compounds Triazoles Secondary carboxylic acid amides Azacyclic compounds Sulfenyl compounds Organochlorides Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - Phenoxy compound - Aryl thioether - P-xylene - Xylene - 1,3-dichlorobenzene - Phenol ether - N-arylamide - Alkyl aryl ether - Chlorobenzene - Halobenzene - Alkylarylthioether - Aryl chloride - Aryl halide - Azole - Heteroaromatic compound - 1,2,4-triazole - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Sulfenyl compound - Thioether - Carboxylic acid derivative - Ether - Azacycle - Organosulfur compound - Organohalogen compound - Hydrocarbon derivative - Organochloride - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Organooxygen compound - 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