Safety of 3,4,5-Trichloropyridine. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 3,4,5-Trichloropyridine, is researched, Molecular C5H2Cl3N, CAS is 33216-52-3, about A novel reagent combination for the oxidation of highly electron deficient pyridines to N-oxides: trifluoromethanesulfonic anhydride/sodium percarbonate. Author is Zhu, Xizhen; Kreutter, Kevin D.; Hu, Huaping; Player, Mark R.; Gaul, Micheal D..
A novel reagent combination, Tf2O/Na2CO3.1.5H2O2, was developed for the oxidation of highly electron-deficient pyridines to their corresponding N-oxides. The N-oxidation reaction, utilizing the in-situ generated peracid, proceeds under mild conditions that allow for a number of functional groups and substitution patterns on the pyridine ring.
There is still a lot of research devoted to this compound(SMILES：C1=NC=C(C(=C1Cl)Cl)Cl)Safety of 3,4,5-Trichloropyridine, and with the development of science, more effects of this compound(33216-52-3) can be discovered.
Reference:
Bromide – Wikipedia,
bromide – Wiktionary