Compound Identification
SMILES
[O-][N+](=O)C1=CC=C(C=CC(=O)N2C3=CC=CC=C3C3=CC=CC=C23)C=C1
InChIKey
InChIKey=LWPHUTVBYVZKQG-UHFFFAOYSA-N
Formula
C21H14N2O3
Mass
342.354
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Indoles and derivatives
-
Subclass
Carbazoles
- Level 5 N-acylcarbazoles
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Subclass
Carbazoles
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Class
Indoles and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Indoles and derivatives
Subclass
Carbazoles
Intermediate Tree Nodes
Not available
Direct Parent
N-acylcarbazoles
Alternative Parents
Cinnamic acids and derivatives Indoles Nitrobenzenes Styrenes Nitroaromatic compounds Substituted pyrroles Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives Organic salts Organonitrogen compounds Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
N-acylcarbazole - Cinnamic acid or derivatives - Indole - Nitrobenzene - Nitroaromatic compound - Styrene - Monocyclic benzene moiety - Substituted pyrrole - Benzenoid - Heteroaromatic compound - Pyrrole - C-nitro compound - Organic nitro compound - Azacycle - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic salt - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic cation - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as n-acylcarbazoles. These are aromatic heteropolycyclic compounds containing a carbazole moiety, which is N-acylated.
External Descriptors
Not available