Metal ions and biological action. XXXIV. The complex-forming ability of some pyridylcarbinols was written by Luz, W. D.;Fallab, S.;Erlenmeyer, H.. And the article was included in Helvetica Chimica Acta in 1955.Quality Control of 6-Methyl-2-pyridinemethanol This article mentions the following:
Reaction of 2-ethylpyridine and H2O2, and acetylation of the product give an Ac derivative b13 106-8° which hydrolyzes to give 36% 2-pyridylmethylcarbinol (I), b12 95-7°. MeMgI and 2-C6H4NCHO give 62% I. LiAlH4 and Et pipecolinate give 2-piperidylcarbinol, m. 60° (picrate m. 128-9.5°). HOCH2CH2NH2 and II do not form complexes with bivalent Cu or Ni ions. 2-Pyridylcarbinol is almost as strong a complexing agent as is oxine. Introduction of a Me group as in I decreases complex formation. In 2-(6-methylpyridyl)carbinol complex formation fails, probably owing to steric factors. In the experiment, the researchers used many compounds, for example, 6-Methyl-2-pyridinemethanol (cas: 1122-71-0Quality Control of 6-Methyl-2-pyridinemethanol).
6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. 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.Quality Control of 6-Methyl-2-pyridinemethanol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts