Related Products of 24034-73-9, The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 24034-73-9, name is (2E,6E,10E)-3,7,11,15-Tetramethylhexadeca-2,6,10,14-tetraen-1-ol. This compound has unique chemical properties. The synthetic route is as follows.
Geranylgeraniol (600 mg, 2.07 mmol) and 15 mE of anhydrous tetrahydroffiran were added to a rubber septum coyered, oven-dried 50 mE round-bottom flask with a magneticstirring bar and a nitrogen inlet. The solution was stirred andcooled to -45 C. Upon cooling of this solution, methanesulfonyl chloride (207.5 pL, 2.67 mmol) was added slowlyvia syringe to the reaction flask. Over a 5-minute period,574.74 jiL of triethylamine was then added via syringe. Theresulting suspension was stirred for 45 minutes at -45 C. Asolution of lithium bromide (717.5mg, 8.26 mmol) inS mE oftetrahydroffiran was added dropwise via syringe. The suspen10 sion was warmed to 0 C. and stirred for 1 hout The reactionmixture was poured into 8 mE of iced water and the aqueouslayer was extracted with ice-cold diethyl ether (3×4 mE). Thecombined organic extracts were washed with ice-cold saturated NaHCO3 (10 mE) and brine (10 mE), and dried overanhydrous Mg504. The organic layer was filtered and concentrated in vacuo to obtain the crude geranylgeranyl bromide, which was then used immediately for the following stepwithout thrther purifications.
According to the analysis of related databases, 24034-73-9, the application of this compound in the production field has become more and more popular.
Reference:
Patent; Wellesley College; Carrico-Moniz, Dora; (19 pag.)US9388155; (2016); B1;,
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