Changes in LD50 of parathion and heptachlor following turpentine pretreatment was written by Sperling, Frederick;Ewenike, Helenah K. U.;Farber, Theodore. And the article was included in Environmental Research in 1972.Application In Synthesis of rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate This article mentions the following:
Stimulation of male rat microsomal enzymes by pretreatment with oral turpentine (1.8 mg/kg/day for 3 days) resulted in reduced hexobarbital sleeping time, reduced parathion (I) [56-38-2] toxicity, and increased heptachlor (II) [76-44-8] toxicity. Hexobarbital hydroxylase [9078-77-7], p-aminophenol aniline hydroxylase [9012-80-0], aminopyrine demethylase [9037-69-8], and benzpyrene hydroxylase [9037-52-9] were stimulated. α-Pinene [80-56-8] and β-pinene [127-91-3] vaporized from turpentine had no effect on hexobarbital sleeping or I mortality but increased II mortality and benzpyrene hydroxylation. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Application In Synthesis of rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate).
rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) 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. 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.Application In Synthesis of rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts