Compound Identification
SMILES
Cl.[O-][N+](=O)C1=CC2=C3C(C=CC=C3C(=O)N(CCNCCCNC(=O)C3=CC(=CC=C3)N3C(=O)C4=CC=CC5=CC(=CC(C3=O)=C45)[N+]([O-])=O)C2=O)=C1
InChIKey
InChIKey=WWDCYGFOILPWBP-UHFFFAOYSA-N
Formula
C36H27ClN6O9
Mass
723.1
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Benzenoids
-
Class
Naphthalenes
- Subclass Nitronaphthalenes
-
Class
Naphthalenes
-
Superclass
Benzenoids
Kingdom
Organic compounds
Superclass
Benzenoids
Class
Naphthalenes
Subclass
Nitronaphthalenes
Intermediate Tree Nodes
Not available
Direct Parent
Nitronaphthalenes
Alternative Parents
Isoquinolones and derivatives Benzamides Benzoyl derivatives Nitroaromatic compounds N-substituted carboxylic acid imides Secondary carboxylic acid amides Amino acids and derivatives Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Dialkylamines Organic oxoazanium compounds Organooxygen compounds Hydrocarbon derivatives Hydrochlorides Organic zwitterions Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2-nitronaphthalene - Isoquinolone - Benzamide - Benzoic acid or derivatives - Nitroaromatic compound - Benzoyl - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - Carboxylic acid imide - Amino acid or derivatives - Organic nitro compound - Carboxamide group - C-nitro compound - Secondary carboxylic acid amide - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Secondary aliphatic amine - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Secondary amine - Organic oxygen compound - Organic salt - Organic oxide - Hydrocarbon derivative - Amine - Hydrochloride - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Organic zwitterion - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as nitronaphthalenes. These are polycyclic aromatic compounds containing a naphthalene moiety substituted by one or more nitro groups.
External Descriptors
Not available