Compound Identification
SMILES
CCOC1=C(O)C(Br)=CC(=C1)C1NC(=O)NC(C)=C1C(=O)NC1=C(C)C=C(C)C=C1
InChIKey
InChIKey=SHQSHJPLXLPSSZ-UHFFFAOYSA-N
Formula
C22H24BrN3O4
Mass
474.355
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 Phenoxy compounds Phenol ethers O-bromophenols N-arylamides Pyrimidones Alkyl aryl ethers Bromobenzenes Aryl bromides Hydropyrimidines Vinylogous amides Ureas Secondary carboxylic acid amides Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organobromides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - 2-halophenol - 2-bromophenol - Phenol ether - N-arylamide - Xylene - M-xylene - Phenoxy compound - Bromobenzene - Pyrimidone - Phenol - Halobenzene - Alkyl aryl ether - Aryl halide - Pyrimidine - Aryl bromide - Hydropyrimidine - 1,2,3,4-tetrahydropyrimidine - Vinylogous amide - Carboxamide group - Urea - Secondary carboxylic acid amide - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Ether - Organooxygen compound - Carbonyl group - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organobromide - Organohalogen 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