Compound Identification
SMILES
CNC(=O)C1=C(C)N=C2SCCCN2C1C1=CC=C(NC(=O)COC2=CC=C(Cl)C=C2)C=C1
InChIKey
InChIKey=MLGDRKXVTJOVGY-UHFFFAOYSA-N
Formula
C24H25ClN4O3S
Mass
485.0
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
Phenoxy compounds Phenol ethers N-arylamides Alkyl aryl ethers Chlorobenzenes Thiazinanes Aryl chlorides Hydropyrimidines Secondary carboxylic acid amides Isothioureas Carboximidamides Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Hydrocarbon derivatives Organochlorides Carbonyl compounds Organic oxides Amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Anilide - Phenoxy compound - N-arylamide - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Hydropyrimidine - 1,6-dihydropyrimidine - 1,3-thiazinane - Carboxamide group - Isothiourea - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Ether - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic oxygen compound - Amine - Organic nitrogen compound - Organic oxide - Carbonyl group - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic 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