Why do aromatic interactions matter of compound: 1127-45-3

Although many compounds look similar to this compound(1127-45-3)Application In Synthesis of 8-Hydroxyquinoline 1-oxide, numerous studies have shown that this compound(SMILES:OC1=CC=CC2=CC=C[N+]([O-])=C12), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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 Oxidation of 1-naphthol and related phenols with hydrogen peroxide and potassium superoxide catalyzed by 5,10,15,20-tetraarylporphyrinatoiron(III) chlorides in different reaction conditions, published in 1999-01-08, which mentions a compound: 1127-45-3, Name is 8-Hydroxyquinoline 1-oxide, Molecular C9H7NO2, Application In Synthesis of 8-Hydroxyquinoline 1-oxide.

Reaction of 1-naphthol and related phenols with hydrogen peroxide catalyzed by 5,10,15,20-tetra(pentafluorophenyl)porphyrinatoiron(III) chloride gives quinones and oxidative coupling products, whereas the reaction of naphthols with hydrogen peroxide catalyzed by 5,10,15,20-tetramesitylporphyrinatoiron(III) chloride gives the above products along with quinone epoxides in moderate yields. The reaction of quinone with potassium superoxide catalyzed by Me12TPPFe(III)Cl and p-MeOTPPFe(III)Cl give higher yields of quinone epoxides than the reaction of quinone with hydrogen peroxide catalyzed by 5,10,15,20-tetraarylporphyrinatoiron(III) chlorides.

Although many compounds look similar to this compound(1127-45-3)Application In Synthesis of 8-Hydroxyquinoline 1-oxide, numerous studies have shown that this compound(SMILES:OC1=CC=CC2=CC=C[N+]([O-])=C12), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider