Proton and carbon-13 NMR study of substituted 3-hydroxypyridines was written by De Kowalewski, D. G.;De Los Santos, C.. And the article was included in Journal of Molecular Structure in 1990.Related Products of 15128-90-2 This article mentions the following:
The additivity of 13C chem. shifts can be used to differentiate the phenolic from the zwitterionic structure in 3-hydroxypyridines; the additivity of 1JCH values cannot be used for this purpose. In the experiment, the researchers used many compounds, for example, 3-Hydroxy-6-methyl-2-nitropyridine (cas: 15128-90-2Related Products of 15128-90-2).
3-Hydroxy-6-methyl-2-nitropyridine (cas: 15128-90-2) belongs to pyridine derivatives. Pyridine is diamagnetic and has a diamagnetic susceptibility of â?8.7 à 10â? cm3·molâ?.The molecular electric dipole moment is 2.2 debyes. The standard enthalpy of formation is 100.2 kJ·molâ? in the liquid phase and 140.4 kJ·molâ? in the gas phase. Pyridine groups exist in countless molecules, and their applications include catalysis, drug design, molecular recognition, and natural product synthesis.Related Products of 15128-90-2