Compound Identification
SMILES
[NH2-].[NH2-].[Cu+].[Cu+].[Cu++].Cl[Cu].N=[N+]=[N-].N=[N+]=[N-].[N-]=[N+]=[N-].C1CN=C(C1)C1[N-]C(=CC=C1)C1=NCCC1
InChIKey
InChIKey=YPOIEDUUTVNMIU-UHFFFAOYSA-M
Formula
C13H22ClCu4N14
Mass
664.05
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Pyridines and derivatives
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Subclass
Hydropyridines
- Level 5 Dihydropyridines
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Subclass
Hydropyridines
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Class
Pyridines and derivatives
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Pyridines and derivatives
Subclass
Hydropyridines
Intermediate Tree Nodes
Not available
Direct Parent
Dihydropyridines
Alternative Parents
Pyrrolines Organic azides Ketimines Propargyl-type 1,3-dipolar organic compounds Organic metal halides Carbene-type 1,3-dipolar compounds Azacyclic compounds Organic copper salts Hydrocarbon derivatives Organic cations
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Dihydropyridine - Pyrroline - Ketimine - Organic azide - Organic metal halide - Azacycle - Propargyl-type 1,3-dipolar organic compound - Carbene-type 1,3-dipolar compound - Organic 1,3-dipolar compound - Organic transition metal salt - Organic metal salt - Imine - Hydrocarbon derivative - Organic salt - Organonitrogen compound - Organic copper salt - Organic nitrogen compound - Organic cation - Aliphatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as dihydropyridines. These are compounds containing a dihydropyridine moiety, which is a semi-saturated pyridine derivative with two double bonds.
External Descriptors
Not available