Koval’skaya, S. S. et al. published their research in Khimiya Prirodnykh Soedinenii in 1989 | CAS: 2451-01-6

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. 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.SDS of cas: 2451-01-6

Stereoselective synthesis of N,N’-diacyl-p-menthan-1,8-diamines was written by Koval’skaya, S. S.;Kozlov, N. G.;Tikhonova, T. S.. And the article was included in Khimiya Prirodnykh Soedinenii in 1989.SDS of cas: 2451-01-6 This article mentions the following:

Reaction of terpin hydrate with RCN (R = Me, ClCH2, Me2CH, Ph) under Ritter reaction conditions stereoselectively leads to the formation of isomeric cis– and trans–N,N‘-diacyl-p-menthane-1,8-diamines in a 1:4 ratio. Structures were confirmed by proton and 13C NMR spectroscopy. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6SDS of cas: 2451-01-6).

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. 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.SDS of cas: 2451-01-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts