Safety of 3,5-Dimethyl-1H-pyrazole. In 2019.0 CHEM HETEROCYCL COM+ published article about DIRECT FUNCTIONALIZATION; OXIDES; BOND; DERIVATIVES; ARYLATION; RADICALS; LITHIUM; AZINES in [Akulov, Alexey A.; Varaksin, Mikhail V.; Charushin, Valery N.; Chupakhin, Oleg N.] Ural Fed Univ, 19 Mira St, Ekaterinburg 620002, Russia; [Varaksin, Mikhail V.; Charushin, Valery N.; Chupakhin, Oleg N.] Russian Acad Sci, Ural Branch, Postovsky Inst Organ Synth, 22 S Kovalevskoi,20 Akad Skaya St, Ekaterinburg 620990, Russia in 2019.0, Cited 28.0. The Name is 3,5-Dimethyl-1H-pyrazole. Through research, I have a further understanding and discovery of 67-51-6.
We report the first example of the direct nucleophilic C-H functionalization of cyclic aldonitrone, a derivative of 2H-imidazole 1-oxide, with 1H-imidazole and 3,5-dimethylpyrazole rings using oxidative C-N cross-coupling reactions in the presence of palladium(II) catalyst. The obtained new bisheterocyclic N-oxides may be of interest as molecules with potential biological activity and as functional organic materials.
Safety of 3,5-Dimethyl-1H-pyrazole. Bye, fridends, I hope you can learn more about C5H8N2, If you have any questions, you can browse other blog as well. See you lster.
Reference:
Pyrazole – Wikipedia,
,Pyrazoles – an overview | ScienceDirect Topics