Abele, E. et al. published their research in Khimiya Geterotsiklicheskikh Soedinenii in 1988 | CAS: 4783-68-0

2-Phenoxypyridine (cas: 4783-68-0) belongs to pyridine derivatives. Pyridine has a dipole moment and a weaker resonant stabilization than benzene (resonance energy 117 kJ·mol� in pyridine vs. 150 kJ·mol� in benzene). Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals.Quality Control of 2-Phenoxypyridine

Synthesis of phenoxypyridines under phase transfer catalysis conditions was written by Abele, E.;Gol’dberg, Yu. Sh.;Gavars, M.;Gaukhman, A. P.;Shimanskaya, M. V.. And the article was included in Khimiya Geterotsiklicheskikh Soedinenii in 1988.Quality Control of 2-Phenoxypyridine This article mentions the following:

Reaction of halopyridines with PhOM (M = Na, K) in a two-phase liquid-solid catalytic system gave phenoxypyridine. With polyhalopyridines, substitution occurred at the α- and γ-positions. Reaction of o-(KO)2C6H4 with 2,3,5,6-tetrabromopyridine gave azaphenoxane I. In the experiment, the researchers used many compounds, for example, 2-Phenoxypyridine (cas: 4783-68-0Quality Control of 2-Phenoxypyridine).

2-Phenoxypyridine (cas: 4783-68-0) belongs to pyridine derivatives. Pyridine has a dipole moment and a weaker resonant stabilization than benzene (resonance energy 117 kJ·mol� in pyridine vs. 150 kJ·mol� in benzene). Several pyridine derivatives play important roles in biological systems. While its biosynthesis is not fully understood, nicotinic acid (vitamin B3) occurs in some bacteria, fungi, and mammals.Quality Control of 2-Phenoxypyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem