Yahkind, A. L. et al. published their research in Progress in Organic Coatings in 2010 | CAS: 115-84-4

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Computed Properties of C9H20O2

Polyols based on isocyanates and melamines and their applications in 1K and 2K coatings was written by Yahkind, A. L.;Paquet, D. A.;Parekh, D. V.;Stine, C. L.;van der Ven, L. G. J.. And the article was included in Progress in Organic Coatings in 2010.Computed Properties of C9H20O2 The following contents are mentioned in the article:

Polyurethane polyols (PUPOs) and melamine polyols (MEPOs), invented by AkzoNobel Coatings, offer valuable alternatives to the commonly used polyester and acrylic polyols and new formulating tools for the development of novel coatings. The resin chem. is based on the predominantly selective reactivity of α,β- and α,γ-diols with commonly used polyisocyanate and melamine formaldehyde crosslinkers. The resulting low mol. weight, hydroxyl functional resins are suitable for use in low VOC coatings. By choosing the appropriate crosslinker, diol, and modifier, the chem. structures of these resins can be altered to obtain the desired properties of the coatings. Synthesis methods for novel PUPOs and MEPOs and properties of one component and two component coatings containing them are described. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Computed Properties of C9H20O2).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Computed Properties of C9H20O2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts