Johns, I. B. et al. published their research in Journal of Chemical and Engineering Data in 1962 | CAS: 4783-68-0

2-Phenoxypyridine (cas: 4783-68-0) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Many analogues of pyridine are known where N is replaced by other heteroatoms . Substitution of one C–H in pyridine with a second N gives rise to the diazine heterocycles (C4H4N2), with the names pyridazine, pyrimidine, and pyrazine.Safety of 2-Phenoxypyridine

Thermal stability of some organic compounds was written by Johns, I. B.;McElhill, E. A.;Smith, J. O.. And the article was included in Journal of Chemical and Engineering Data in 1962.Safety of 2-Phenoxypyridine This article mentions the following:

Decomposition temps, as defined previously (Ind. Eng. Chem., Prod. Res. Develop. 1, 2-6(1962)) are given for approx. 90 compds, in the classes: aromatic, substituted aromatic, heterocyclic, s-triazine, Si, B, P, and F compounds Decomposition products of 42 of the compounds are identified. Vapor pressure data for 16 of the compounds are given as constants in the equation log Pmm = b – a/T. In the experiment, the researchers used many compounds, for example, 2-Phenoxypyridine (cas: 4783-68-0Safety of 2-Phenoxypyridine).

2-Phenoxypyridine (cas: 4783-68-0) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Many analogues of pyridine are known where N is replaced by other heteroatoms . Substitution of one C–H in pyridine with a second N gives rise to the diazine heterocycles (C4H4N2), with the names pyridazine, pyrimidine, and pyrazine.Safety of 2-Phenoxypyridine

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem