[Pd].[Pd].NC1=NC2=C(C=C1)C=CC(=O)[N-]2.NC1=NC2=C(C=C1)C=CC(=O)[N-]2.C1CCC([N-]C1)C1CCCC[N-]1.C1CCC([N-]C1)C1=CC=CC[N-]1

InChIKey=MVQCVMFJQQIVIN-UHFFFAOYSA-L

C36H44N10O2Pd2

861.66

Organic compounds

Organoheterocyclic compounds

Diazanaphthalenes

Naphthyridines

Not available

Naphthyridines

Pyridinones Dihydropyridines Aminopyridines and derivatives Piperidines Imidolactams Heteroaromatic compounds Organic transition metal salts Carbene-type 1,3-dipolar compounds Azacyclic compounds Primary amines Organooxygen compounds Organic oxides Hydrocarbon derivatives Organic anions

Not available

Naphthyridine - Aminopyridine - Dihydropyridine - Pyridinone - Hydropyridine - Piperidine - Imidolactam - Pyridine - Heteroaromatic compound - Azacycle - Organic transition metal salt - Carbene-type 1,3-dipolar compound - Primary amine - Organic oxide - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Organic oxygen compound - Amine - Hydrocarbon derivative - Organic anion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as naphthyridines. These are compounds containing a naphthyridine moiety, a naphthalene in which a carbon atom has been replaced by a nitrogen in each of the two rings. The naphthyridine skeleton can also be described as an assembly two fused pyridine rings, which do not share their nitrogen atom.

Not available