Compound Identification
SMILES
CC(C)C(N)C1=NN=C(O1)SCC(=O)NC1=CC=C(Br)C=C1
InChIKey
InChIKey=MWTBNPGNOCCGCS-UHFFFAOYSA-N
Formula
C14H17BrN4O2S
Mass
385.28
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 Alkylarylthioethers Aralkylamines Bromobenzenes Aryl bromides 1,3,4-oxadiazoles Heteroaromatic compounds Secondary carboxylic acid amides Amino acids and derivatives Sulfenyl compounds Azacyclic compounds Oxacyclic compounds Hydrocarbon derivatives Carbonyl compounds Organobromides Monoalkylamines Organic oxides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Anilide - Aryl thioether - N-arylamide - Bromobenzene - Halobenzene - Alkylarylthioether - Aralkylamine - Aryl bromide - Aryl halide - 1,3,4-oxadiazole - Azole - Oxadiazole - Heteroaromatic compound - Secondary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Sulfenyl compound - Thioether - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Primary amine - Organohalogen compound - Primary aliphatic amine - Hydrocarbon derivative - Organobromide - Organonitrogen compound - Carbonyl group - Organic oxide - Amine - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur 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