Compound Identification
SMILES
IC1=CC=C(NC(=O)C2=CC3=C(C=C2)C(=O)N2CCCCCC2=N3)C=C1
InChIKey
InChIKey=NXCNFUCWAPONMC-UHFFFAOYSA-N
Formula
C20H18IN3O2
Mass
459.287
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Benzenoids
-
Class
Benzene and substituted derivatives
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Subclass
Anilides
- Level 5 Aromatic anilides
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Subclass
Anilides
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Class
Benzene and substituted derivatives
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Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Benzene and substituted derivatives
Subclass
Anilides
Intermediate Tree Nodes
Not available
Direct Parent
Aromatic anilides
Alternative Parents
Quinazolines Pyrimidones Iodobenzenes Azepines Azepanes N-acyl amines Hydropyrimidines Heteroaromatic compounds Lactams Vinyl iodides Propargyl-type 1,3-dipolar organic compounds Iodoalkenes Carboxylic acid amides Carboximidamides Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organoiodides Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Aromatic anilide - Diazanaphthalene - Quinazoline - Pyrimidone - Iodobenzene - Halobenzene - Azepine - Azepane - Pyrimidine - N-acyl-amine - 1,6-dihydropyrimidine - Hydropyrimidine - Heteroaromatic compound - Lactam - Carboxamide group - Azacycle - Iodoalkene - Haloalkene - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Vinyl iodide - Vinyl halide - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organoiodide - Organohalogen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as aromatic anilides. These are aromatic compounds containing an anilide group in which the carboxamide group is substituted with an aromatic group. They have the general structure RNC(=O)R', where R= benzene, and R = aryl group.
External Descriptors
Not available