SDS of cas: 18362-64-6. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 2,6-Dimethyl-3,5-heptanedione, is researched, Molecular C9H16O2, CAS is 18362-64-6, about Thermodynamic functions of enolization of aliphatic β-diketone. Author is Calmon, Jean P..
The following data were determined (β-diketone, % enol form at 33°C. equilibrium constant for the keto-enol tautomer at 33°C., enthalpy of enolization -ΔH in kcal./mole, and entropy of enolization -ΔS at 33°C. in cal./mole/°K.): Ac2CH2, 79.5, 3.89, 2.8, 6.45; AcCH2COEt, 80.5, 4.09, 3.0, 7.0; iso-PrCOCH2Ac, 89, 7.88, 3.2, 6.35; iso-BuCOCH2Ac, 90, 8.87, 3.3, 6.45; tert-BuCOCH2Ac, 93.5, 14.30, 3.9, 7.45; tert-BuCH2COCH2Ac, 94, 15.65, 3.45, 5.8; iso-BuCOCH2COEt, 90.5, 9.81, 3.7, 7.55; iso-BuCOCH2COPr, 92, 11.40, 3.4, 6.3; iso-BuCOCH2COPr-iso, 95, 20.30, 4.45, 8.55; (iso-BuCO)2CH2, 93.5, 14.60, 3.3, 5.8; (iso-PrCO)2CH2, 94, 15.95, 3.7, 6.6; tert-BuCOCH2COPr-iso, 96, 23.15, 4.65, 8.95; (tert-BuCO)2CH2, 98.5, 58.9, 4.9, 8.25. The data were determined from the N.M.R. spectra of the β-diketone. The variations in the entropies are attributed to resonance stabilization of the enol form and to the steric effects of the substituents which destabilize the keto form. The strong neg. entropy is explained by a chelated enolic structure which is more rigid than the diketo form.
There are many compounds similar to this compound(18362-64-6)SDS of cas: 18362-64-6. if you want to know more, you can check out my other articles. I hope it will help you，maybe you’ll find some useful information.
Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica