Compound Identification
SMILES
CC1=CC=C(C=C1)N1N=C(SC11S\C(=C\C2=CC=C(Br)C=C2)C(=O)N1C1=CC=CC=C1)C(=O)NC1=CC=CC=C1
InChIKey
InChIKey=XWXYBPRJSJCGQJ-NHFJDJAPSA-N
Formula
C31H23BrN4O2S2
Mass
627.58
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 Toluenes Bromobenzenes Aryl bromides Thiazolidines Thiadiazolines Tertiary carboxylic acid amides Thioenol ethers Secondary carboxylic acid amides Lactams Azacyclic compounds Hydrazones Carbonyl compounds Organic oxides Organobromides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Anilide - N-arylamide - Bromobenzene - Halobenzene - Toluene - Aryl bromide - Aryl halide - Tertiary carboxylic acid amide - Thiadiazoline - Thiazolidine - Carboxamide group - Lactam - Secondary carboxylic acid amide - Thioenolether - Hydrazone - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organic oxygen compound - Organic oxide - 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