Compound Identification
SMILES
CN1C(COC2=CC=CC(C)=C2)=NN=C1SCC(=O)NC1=C(Br)C=C(C)C(C)=C1
InChIKey
InChIKey=QNRYLEVGZOWEBV-UHFFFAOYSA-N
Formula
C21H23BrN4O2S
Mass
475.41
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
o-Xylenes Phenoxy compounds Phenol ethers N-arylamides Toluenes Alkyl aryl ethers Alkylarylthioethers Bromobenzenes Aryl bromides Triazoles Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Sulfenyl compounds Carbonyl compounds Organic oxides Organobromides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - Phenol ether - Phenoxy compound - Aryl thioether - N-arylamide - O-xylene - Xylene - Alkyl aryl ether - Toluene - Halobenzene - Alkylarylthioether - Bromobenzene - Aryl bromide - Aryl halide - 1,2,4-triazole - Heteroaromatic compound - Azole - Carboxamide group - Secondary carboxylic acid amide - Azacycle - Organoheterocyclic compound - Carboxylic acid derivative - Ether - Sulfenyl compound - Thioether - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organohalogen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Organosulfur 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