What unique challenges do researchers face in Phenyl(pyridin-2-yl)methanone

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Safety of Phenyl(pyridin-2-yl)methanone. Recently I am researching about GEM-DISUBSTITUTED ALKENES; C=C BOND-CLEAVAGE; C DOUBLE-BOND; SELECTIVE OXIDATION; EFFICIENT; HYDROGENATION; OZONOLYSIS; QUINOLINES; CATALYSTS; COMPLEX, Saw an article supported by the 111 ProjectMinistry of Education, China – 111 Project [D20015]; Natural Science Foundation of Hubei Province of ChinaNatural Science Foundation of Hubei Province [2018CFB241]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Yu, T; Guo, MQ; Wen, SMM; Zhao, RR; Wang, JL; Sun, YL; Liu, QX; Zhou, HF. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone

A simple, and practical oxidative scission of aromatic olefins to carbonyl compounds using O-2 as the sole oxidant with poly(ethylene glycol) dimethyl ether as a benign solvent has been developed. A wide range of monosubstituted, gem-disubstituted, 1,2-disubstituted, trisubstituted and tetrasubstituted aromatic olefins was successfully converted into the corresponding aldehydes and ketones in excellent yields even with gram-scale reaction. Some control experiments were also conducted to support a possible reaction pathway.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem