Some low molecular weight alcohols of industrial importance are produced by the addition of water to alkenes. 647-42-7, formula is C8H5F13O, Ethanol, isopropanol, 2-butanol, and tert-butanol are produced by this general method. Two implementations are employed, the direct and indirect methods. Synthetic Route of 647-42-7
Xiang, Fan;Zong, Yakun;Chen, Mingqiang;Li, Zhanxiong research published 《 Preparation of super-hydrophobic cotton fabrics with the controllable roughening fiber surface by carbene polymerization grafting》, the research content is summarized as follows. Superhydrophobic cotton fabrics were successfully prepared by grafting modification of cotton fabrics through carbene polymer induced crystallization and self-assembly. The structures and properties of grafted polymer crystals on the surface of cotton fabrics were examined by SEM, FT-IR and NMR. The surface grafting positions with diazo active groups were pre-constructed on the fibers. The 3,3,4,4,5,5,6,6,6-nonfluorohexyl diazoacetate and 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl diazoacetate were synthesized as precursors followed by carbene grafting to fiber. Under different reaction conditions, the polymer crystallized on the fiber surface and produced different morphologies. When 3,3,4,4,5,5,6,6,6-nonfluorohexyl diazoacetate was used as the precursor and THF as the solvent, the grafted cotton fabric exhibited excellent hydrophobic properties with a water contact angle of 152°. When 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl diazoacetate was used as the grafting precursor, THF or THF/EtOH mixed solvent was used as the reaction medium, the contact angle of the as-prepared cotton fabric to water was measured to be 151° and 154°, resp. During the carbene grafting polymerization, the solvent has a significant influence on the morphol. of the grafted polymer. The WCA and EDS results suggest that the synergistic effect between the rough structure of the grafted cotton fabric surface and the low surface energy of fluorine element made the fabric super-hydrophobic.
647-42-7, 3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctan-1-ol, also known as 1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol , is a useful research compound. Its molecular formula is C8H5F13O and its molecular weight is 364.1 g/mol. The purity is usually 95%.
1H,1H, 2H, 2H-Tridecafluoro-1-n-octanol is a material used to improve nanotube composites. It is also used in the synthesis of a recyclable fluorous hydrazine carbothioate compound with NCS to catalyze the acetalization of aldehydes.
1H,1H,2H,2H-Tridecafluoro-1-n-octanol is a potent and selective halogenated hydrocarbon. It binds to DNA at the dinucleotide phosphate site, which is an important site for polymerase chain reaction (PCR) activation. 1HFN has been shown to be more effective than other halogenated hydrocarbons in vitro assays on rat liver microsomes. It has been used as an additive in wastewater treatment to remove organic contaminants and metal ions. In vivo studies have been carried out in CD-1 mice to determine the effects of 1HFN on the liver and kidneys; these studies showed no toxicological effects on these organs. 1HFN also has been shown to inhibit enzymes such as cytochrome P450 and monoamine oxidase B that are involved in drug metabolism and may lead to adverse reactions with drugs metabolized by these enzymes., Synthetic Route of 647-42-7
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts