Compound Identification
SMILES
CC(=O)NC1=C(Br)C=C(C=C1)C(C)=NNC1=NCCN1
InChIKey
InChIKey=RCHCDMJIJJRONF-UHFFFAOYSA-N
Formula
C13H16BrN5O
Mass
338.209
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
-
Subclass
Anilides
-
Level 5
Acetanilides
-
Level 6
Haloacetanilides
- Level 7 O-haloacetanilides
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Level 6
Haloacetanilides
-
Level 5
Acetanilides
-
Subclass
Anilides
-
Class
Benzene and substituted derivatives
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Anilides
Intermediate Tree Nodes
Acetanilides - Haloacetanilides
Direct Parent
O-haloacetanilides
Alternative Parents
N-acetylarylamines Bromobenzenes Aryl bromides Imidazolines Acetamides Secondary carboxylic acid amides Guanidines Propargyl-type 1,3-dipolar organic compounds Carboximidamides Azacyclic compounds Organobromides Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
O-haloacetanilide - N-acetylarylamine - N-arylamide - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - 2-imidazoline - Acetamide - Carboxamide group - Guanidine - Secondary carboxylic acid amide - Carboximidamide - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic oxide - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as o-haloacetanilides. These are organic compounds containing an acetamide group conjugated to a phenyl group, which is in turn ortho-substituted with a halogen atom.
External Descriptors
Not available