Derivation of elementary reaction about 1194-22-5

《The proton magnetic resonance spectra and the structure of 4,6-dihydroxypyrimidine and its derivatives》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(6-Hydroxy-2-methylpyrimidin-4(3H)-one)HPLC of Formula: 1194-22-5.

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 1194-22-5, is researched, Molecular C5H6N2O2, about The proton magnetic resonance spectra and the structure of 4,6-dihydroxypyrimidine and its derivatives, the main research direction is DIHYDROXYPYRIMIDINES PMR; PYRIMIDINES PMR; HYDROXYPYRIMIDINES PMR.HPLC of Formula: 1194-22-5.

The proton N.M.R. spectra of 4,6-dihydroxypyrimidine and its 2- and 5-substituted derivatives have been compared with the spectra of their O- and N-methyl derivatives of fixed structures, corresponding to possible tautomeric forms. In a Me2SO medium the compounds exist predominantly in the oxohydroxy form. In aqueous solutions of 4,6-dihydroxypyrimidine and its N-methyl derivatives the bipolar-ionic form with delocalized charges probably predominates. 22 references.

《The proton magnetic resonance spectra and the structure of 4,6-dihydroxypyrimidine and its derivatives》 provides a strategy for the preparation of materials with excellent comprehensive properties, which is conducive to broaden the application field of this compound(6-Hydroxy-2-methylpyrimidin-4(3H)-one)HPLC of Formula: 1194-22-5.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem