Proton-ligand stability constants of substituted ortho-hydroxyacetophenones and ortho-hydroxypropiophenones was written by Kamat, P. V.;Datar, M. G.. And the article was included in Journal of the Indian Chemical Society in 1970.Recommanded Product: 2′,6′-Dihydroxy-4′-methylacetophenone This article mentions the following:
Proton-ligand stability constant of substituted o-hydroxyacetophenones and o-hydroxypropiophenones were determined at 30° by a potentiometric method by the Bjerrum-Calvin titration technique at constant ionic strength ∼0.1M NaClO4. Correlation between the effect and the position of substituents in the benzene nucleus is discussed. In the experiment, the researchers used many compounds, for example, 2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0Recommanded Product: 2′,6′-Dihydroxy-4′-methylacetophenone).
2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 2′,6′-Dihydroxy-4′-methylacetophenone
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts