78210-43-2

Usage

Uses

Used in Chemical Synthesis:
Dipyridin-3-ylmethane is used as a reagent in chemical synthesis for its unique structure and functional groups, which can provide interesting physiochemical properties. Its potential applications in this field are still under investigation.
Used in Research and Development:
Dipyridin-3-ylmethane is used as a research compound in the field of organoheterocyclic chemistry. Its properties and potential applications are being explored to understand its role in various chemical reactions and processes.
Note: Since the detailed applications and uses of DIPYRIDIN-3-YLMETHANE have not been thoroughly researched and documented, the above uses are based on its potential as a reagent and research compound. Further studies are required to establish its specific applications in various industries.

InChI:InChI=1/C11H10N2/c1-3-10(8-12-5-1)7-11-4-2-6-13-9-11/h1-6,8-9H,7H2

Upstream product

• 35779-35-2 di-3-pyridylmethanone 
• 737007-16-8 MBAP 
• 504-29-0 2-aminopyridine 
• 93-60-7 methyl 3-pyridinecarboxylate 
• 626-55-1 3-Bromopyridine 

Downstream Products

• 1355718-60-3 (dipyridin-3-ylmethyl)triphenylphosphonium bromide 

Relevant academic research and scientific papers

Synthesis, characterization, Catalytic and antibacterial activity of two series of dinuclear ruthenium sulphoxide complexes using 5,5'- methylenebis(pyridine) as bis-chelating bridging ligand

The reaction of a new heterocyclic bidentate N containing spacer, (ligand) 5,5'-methylenebis(pyridine) with ruthenium sulphoxide precursors resulted, dinuclear complexes. We herein report three formulations; [{cis,fac-RuCl 2(so)3}2(μ-mbp)].3so; [{trans,mer-RuCl 2(so)3}2(μ-mbp)].3so and [{trans-RuCl 4(so)}2(μ-mbp)]2-[X]2 +; where so = dimethyl-sulfoxide/tetramethylenesulfoxide; mbp = 5,5'-methylenebis(pyridine) and [X]+ = [(dmso)2H] +, Na+ or [(tmso)H]+. These complexes were characterized on the basis of elemental analyses, molar conductance measurement, magnetic susceptibility, FT-IR, 1H-NMR, 13C{1H}-NMR, electronic spectroscopy and FAB-Mass spectrometry. Catalytic activity of these complexes has been investigated in hydrolysis of benzonitrile. All the complexes exhibit good antibacterial activity against gram-negative bacteria Escherichia coli in comparison to Chloramphenicol.

Synthesis and photoluminescent properties of new ceramidine derivatives

A series of new ceramidine derivatives 8a-f has been synthesized in 4-5 steps involving a Wittig reaction of ceramidonine with various triphenylphosphonium bromides. Their UV and photoluminescence (PL) properties are reported. The compounds showed medium to strong PL between 502 and 522 nm at a concentration of 1 × 10-5 M CH2Cl2.

POTASSIUM CHANNEL INHIBITORS

The present invention relates to compounds having the structure useful as potassium channel inhibitors to treat cardiac arrhythmias, and the like.