In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Reaction of oxide radical ion (O·-) with substituted pyrimidines, published in 2002-06-30, which mentions a compound: 1194-22-5, mainly applied to reaction oxide radical substituted pyrimidine oxidizing radical electron transfer; pulse radiolysis reaction oxide radical substituted pyrimidine, Formula: C5H6N2O2.
Pulse radiolysis technique has been used to investigate the reaction of oxide radical ion (O·-) with 4,6-dihydroxy-2-Me pyrimidine (DHMP), 2,4-dimethyl-6-hydroxy pyrimidine (DMHP), 5,6-di-Me uracil (DMU) and 6-Me uracil (MU) in strongly alk. medium. The second-order rate constants for the reaction of O·- with these compounds are in the range 2-5 × 108 dm3 mol-1 s-1. The transient absorption spectra obtained with DHMP have two maxima at 290 and 370 nm and with DMHP have maxima at 310 and 470 nm. The transient spectrum from DMU is characterized by its absorption maxima at 310 and 520 nm and that of MU by its single maximum at 425 nm. The intermediate species were found to react with N,N,N’,N’-tetramethyl-p-phenylenediamine (TMPD) with high G(TMPD·+) values ranged between 3.9 × 10-7 mol J-1 and 4.8 × 10-7 mol J-1. These radicals undergo decay by second-order kinetics (2k/ε = 1.0-1.7 × 106 s-1). The reaction of O·- with the selected pyrimidines is proposed to proceed through a hydrogen abstraction from the Me group forming allyl type radicals. These are mainly oxidizing radicals and hence readily undergo electron transfer reactions with TMPD.
There is still a lot of research devoted to this compound(SMILES：CC1=NC(=CC(N1)=O)O)Formula: C5H6N2O2, and with the development of science, more effects of this compound(1194-22-5) can be discovered.
Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem