63285-53-0

Usage

Structure

A pyridine ring with two attached pyrazole rings at the 2 and 6 positions

Common uses

As a ligand in coordination chemistry to form coordination complexes with metal ions (e.g. copper and cobalt)

Potential applications

Catalysis, development of new materials

Biological activities

Investigation for its role as an inhibitor of various enzymes

Fields of application

Chemistry, materials science, and biochemistry.

Upstream product

• 63285-43-8 1,1'-(2,6-Pyridindiyl)bis<3-(dimethylamino)-2-propen-1-on> 
• 1129-30-2 2,6-Diacetylpyridine 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 

Downstream Products

• 862538-23-6 2,6-Bis-{1-[4-(3-pyridin-2-yl-pyrazol-1-ylmethyl)-benzyl]-1H-pyrazol-3-yl}-pyridine 
• 1315594-59-2 [(2,6-bis(1H-pyrazol-3-yl)pyridine)RuCl(NC₅H₃CH=NSO₂Ph)]Cl 
• 1464008-49-8 2,6-di(1-benzylpyrazol-3-yl)pyridine 

Relevant academic research and scientific papers

New N,N,N-donors resulting in highly active ruthenium catalysts for transfer hydrogenation at room temperature

A series of ruthenium complexes of the general formula [RuCl 2(L)(NNN)] were synthesized starting from tridentate N,N,N-ligands containing pyridine and allylated pyrazole donor groups and [RuCl 2(PPh3)3]. The N,

Asymmetric Catalysis, 77. - New Optically Active Pyrazole Derivatives for Enantioselective Catalysis

Starting from the amines 3-6 and the dipyrazolopyrazinedione 2, the optically active (pyrazolylmethyl)amines 11-14 have been synthesized.Furthermore, the preparation of the (+)-camphor-derived optically active pyrazole 17 is described.Pyrazoles 11-13 and 17 are introduced as chiral building blocks into the 2-(1-pyrazolyl)pyridines 30-33.The optically active compounds 23-25 are formed from 2-pyridine and 2,6-bispyridine, respectively, and (+)-3-(bromomethyl)pinane.The pyrazole derivatives 27-29 contain (+)-(1-phenylethyl)hydrazine as the optically active component.Key Words: Pyrazoles, optically active / Pyridines, 2--, 2,6-bis-, 2-(1-pyrazolyl)-