Compound Identification
SMILES
[Ni].CC1=NC(CNC=C2C=C(C=CC2=O)[N+]([O-])=O)=CC=C1.CC1=NC(CNC=C2C=C(C=CC2=O)[N+]([O-])=O)=CC=C1
InChIKey
InChIKey=HWHRJPDNZVLGRZ-UHFFFAOYSA-N
Formula
C28H26N6NiO6
Mass
601.245
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Pyridines and derivatives
- Subclass 2-pyridylmethylamines
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Class
Pyridines and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyridines and derivatives
Subclass
2-pyridylmethylamines
Intermediate Tree Nodes
Not available
Direct Parent
6-substituted-2-pyridinylmethylamines
Alternative Parents
O-quinomethanes Aralkylamines Methylpyridines Vinylogous amides Heteroaromatic compounds C-nitro compounds Allylamines Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Organic transition metal salts Enamines Dialkylamines Hydrocarbon derivatives Organic zwitterions Organic oxides
Molecular Framework
Not available
Substituents
6-substituted-2-pyridinylmethylamine - O-quinomethane - Quinomethane - Methylpyridine - Aralkylamine - Heteroaromatic compound - Vinylogous amide - Ketone - C-nitro compound - Cyclic ketone - Organic nitro compound - Secondary aliphatic amine - Enamine - Organic oxoazanium - Allylamine - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Organic transition metal salt - Organooxygen compound - Organonitrogen compound - Amine - Hydrocarbon derivative - Organic zwitterion - Organic nitrogen compound - Organic oxygen compound - Organic salt - Organic oxide - Carbonyl group - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as 6-substituted-2-pyridinylmethylamines. These are aromatic heterocyclic compounds contaning a pyridine ring which is substituted at the 2-position with a methylamine, and at the 6-position with any non-hydrogen atom.
External Descriptors
Not available