182319-00-2

Basic information

• Product Name: 2,2'-Bipyridine, 5,5'-diphenyl-
• CAS NO: 182319-00-2
• Molecular Formula: C22H16N2
• Molecular Weight: 308.382
• Mol File: 182319-00-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,2'-Bipyridine, 5,5'-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-Bipyridine, 5,5'-diphenyl-(182319-00-2)
• EPA Substance Registry System: 2,2'-Bipyridine, 5,5'-diphenyl-(182319-00-2)

Safety Data

• Hazardous Substances Data: 182319-00-2(Hazardous Substances Data)

Upstream product

• 1131-48-2 3-phenylpyridine N-oxide 
• 15862-18-7 5,5'-dibromo-2,2'-dipyridyl 
• 98-80-6 phenylboronic acid 
• 107351-82-6 2-bromo-5-phenyl-pyridine 
• 1008-88-4 3-phenylpyridine 

Downstream Products

• 102869-28-3 osmium(II)tris(5,5'-diphenyl-2,2'-bipyridine)⁽²⁺⁾ 

Relevant articles and documents

A spectroscopic study of some substitued tris(diimine) complexes of ruthenium(II) and their reduction products

The electronic absorption and resonance Raman spectra of the parent and one- to six-electron reduction products of tris(5,5'-bis(ethoxycarbonyl)-2,2'-bipyridine)ruthenium(II) and tris(5,5'-bis(phenyl)-2,2'-bipyridine)rythenium(II) indicate that the redox

Mechanistic insights into the potassium: Tert -butoxide-mediated synthesis of N-heterobiaryls

We report herein that symmetrical and non-symmetrical N-heterobiaryls are produced by a potassium tert-butoxide-mediated dimerization of heterocyclic N-oxides. The reaction is scalable and transition metal-free, and can be carried out under thermal and microwave conditions. Preliminary mechanistic studies point to the involvement of radical anionic intermediates arising from the N-oxide substrates and potassium tert-butoxide.