In general, the hydroxyl group makes alcohols polar. Those groups can form hydrogen bonds to one another and to most other compounds. 24034-73-9, formula is C20H34O, Owing to the presence of the polar OH alcohols are more water-soluble than simple hydrocarbons. Methanol, ethanol, and propanol are miscible in water. Butanol, with a four-carbon chain, is moderately soluble. Synthetic Route of 24034-73-9
Hassan, Mohammad M.;Kanagasabai, V.;Nandini, M. S.;Prabhu, K.;Rao, M. R. K.;Kalaivannan, J.;Janaki, C. S. research published 《 The Gc Ms analysis of ethyl acetate extract of one herbal plant, ′Gmelina asiatica′》, the research content is summarized as follows. The present study deals with the GC MS anal. of one medicinal plant, ′Gmelinaasiatica.′Gmelinaasiaticais a wild shrub belonging to family Lamiaceae. Roots, leaves, young shoots of Gmelinaasiatica are considered to be medicinal in traditional medicine. This plant was collected from nearby hills of Chengalpattu, Tamilnadu. The Et acetate extract of the aerial parts of the plant was subjected to GC MS study following standard protocols. It was observed that some very important mols. such as 7-Octadecyne, 2-methyl-, Et 13-methyl-tetradecanoate, Oleic Acid, 3,7,11,15-Tetramethyl-2-hexadecen-1-ol, Me 8,11,14,17-eicosatetraenoate, 2-((Octan-2-yloxy)carbonyl)benzoic acid, Sulfurous acid, Bu heptadecyl ester, trans-Geranylgeraniol, dl-.alpha.-Tocopherol, Oleyl alc., trifluoroacetate, Ursodeoxycholic acid, Stigmasterol, .alpha.-N-Normethadol, beta.-Amyrin, betulin, etc. These mols. have far reaching medicinal roles which correspond to the reports of its medicinal values of Gmelinaasiatica.
24034-73-9, Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. It has a role as a plant metabolite, a volatile oil component and an antileishmanial agent. It is a diterpenoid and a polyprenol.
Geranylgeraniol, a precursor to geranylgeranylpyrophosphate, is an intermediate in the mevalonate pathway. Geranylgeraniol has been shown to prevent bone re-absorption, inhibition of osteoclast formation, and kinase activation in vitro. When working with statins, Geranylgeraniol can reduce the toxicity without inhibiting the cholesterol-producing effects. Geranylgeraniol has been documented to counteract the effects of fluvastatin by inhibiting activation of caspase-1 and production of IL-1. Additionally Geranylgeraniol has been found to induce apoptosis in HL-60 cells.
, Synthetic Route of 24034-73-9
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts