1604-73-5

Usage

Uses

Used in Pharmaceutical Applications:
(2'R,8R)-2',5,6,7',8,8'-hexamethyl-2',8-bis-[(4R,8R)-4,8,12-trimethyl-tridecyl]-1,3',4',8,9,10-hexahydro-2'H-spiro[benzo[1,2-b:4,3-b']dipyran-3(2H),5'-[5H-1]benzopyran]-6'-one is used as a potential pharmaceutical candidate for various applications due to its unique structure and properties.
Used in Materials Science:
(2'R,8R)-2',5,6,7',8,8'-hexamethyl-2',8-bis-[(4R,8R)-4,8,12-trimethyl-tridecyl]-1,3',4',8,9,10-hexahydro-2'H-spiro[benzo[1,2-b:4,3-b']dipyran-3(2H),5'-[5H-1]benzopyran]-6'-one is used as a component in the development of new materials with specific properties, such as improved stability or reactivity.
Used in Organic Synthesis:
(2'R,8R)-2',5,6,7',8,8'-hexamethyl-2',8-bis-[(4R,8R)-4,8,12-trimethyl-tridecyl]-1,3',4',8,9,10-hexahydro-2'H-spiro[benzo[1,2-b:4,3-b']dipyran-3(2H),5'-[5H-1]benzopyran]-6'-one is used as a building block or intermediate in the synthesis of other complex organic compounds for various applications.
Note: The specific applications and reasons mentioned above are hypothetical and provided as examples. Further research and testing would be required to determine the actual properties and potential uses of (2'R,8R)-2',5,6,7',8,8'-hexamethyl-2',8-bis-[(4R,8R)-4,8,12-trimethyl-tridecyl]-1,3',4',8,9,10-hexahydro-2'H-spiro[benzo[1,2-b:4,3-b']dipyran-3(2H),5'-[5H-1]benzopyran]-6'-one.

Upstream product

• 1026734-30-4 2,5,7,8-tetramethyl-8a-[2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6-yloxy]-2-(4,8,12-trimethyltridecyl)-3,4-dihydro-2H,8aH-chromen-6-one 
• 59-02-9 Tocopherol 

Relevant academic research and scientific papers

Effect of α-tocopherol on the hemin-catalyzed decomposition of 1-palmitoyl-2-linoleoyl-3-sn-phosphatodylcholine 13-hydroperoxide in micelles and liposomes

The secondary process of lipid peroxidation produces some toxic aldehydes. Since this process takes place via free radical reaction in lipophilic circumstances, α-tocopherol would suppress the formation of such aldehydes by trapping free-radical intermedi

Vitamin E chemistry. studies into initial oxidation intermediates of α-tocopherol: Disproving the involvement of 5a-C-centered "chromanol methide" radicals

(Chemical Equation Presented) Contrary to concepts handed down in the literature from the early days of vitamin E research, one-electron oxidation of vitamin E does not involve 5a-C-centered radicals. A combined approach of analytical techniques, in particular electron paramagnetic resonance spectroscopy (EPR), organic synthesis of special derivatives, isotopic labeling, kinetic studies, and computational chemistry was used to re-evaluate the one-electron and two-electron oxidation chemistry of α-tocopherol (α-toc). EPR in combination with 5a-13C-labeled compounds provided no indication of the involvement of 5a-C-centered radicals. Oxidation of special tocopherol derivatives were used to disprove the occurrence of 5a-C-centered one-electron intermediates. Additionally it was shown that those vitamin E reactions that were commonly evoked to plead for the involvement of C-centered tocopheryl radicals actually proceeded via heterolytic, i.e., non-radical, intermediates. The results will help to clear widely spread misunderstandings about the chemistry of vitamin E and will have mechanistic implications for the synthesis of tocopherol-based supramolecular structures and 5a-substituted α-tocopherol derivatives.