Chemical Properties and Facts of 1008-89-5

There is still a lot of research devoted to this compound(SMILES:C1(C2=CC=CC=C2)=NC=CC=C1)Safety of 2-Phenylpyridine, and with the development of science, more effects of this compound(1008-89-5) can be discovered.

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called A Mild Method for Electrochemical Reduction of Heterocyclic N-Oxides, published in 2020-06-01, which mentions a compound: 1008-89-5, Name is 2-Phenylpyridine, Molecular C11H9N, Safety of 2-Phenylpyridine.

Deoxygenation of heteroaromatic N-oxides is commonly accomplished using chem. or enzymic methods. In this work, we report on an expedient protocol for electrochem. reduction of pyridine N-oxide derivatives under mild conditions. A diverse range of mono- and bis N-oxides were converted into the corresponding nitrogen bases in good yields. Importantly, the method is highly selective towards N-oxides and tolerates challenging halo and nitro substituents in the heteroaromatic ring. Thus, e.g., 2-phenylpyridine N-oxide → 2-phenylpyridine (89% isolated) by carring out the reaction in an undivided electrochem. cell with two graphite electrodes in 1:1 MeCN/water mixture using LiBF4 as supporting electrolyte.

There is still a lot of research devoted to this compound(SMILES:C1(C2=CC=CC=C2)=NC=CC=C1)Safety of 2-Phenylpyridine, and with the development of science, more effects of this compound(1008-89-5) can be discovered.

Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles