Anderton, K. et al. published their research in Journal of the Chemical Society in 1965 | CAS: 1634-34-0

2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 1634-34-0

The chemistry of β-polycarbonyl compounds. I. Cyclization to furan and coumarin derivatives was written by Anderton, K.;Rickards, R. W.. And the article was included in Journal of the Chemical Society in 1965.HPLC of Formula: 1634-34-0 This article mentions the following:

In the presence of a base and the appropriate halogen, heptane-2,4,6-trione undergoes intramolecular cyclization to furans, which exist exclusively as the enolic tautomers. Intermolecular condensation of ethyl acetoacetate in the presence of sodium ethoxide leads to a coumarin. In the experiment, the researchers used many compounds, for example, 2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0HPLC of Formula: 1634-34-0).

2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 1634-34-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts