85877-79-8 | Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane

CAS:85877-79-8 | Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane ,Description

Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane (TMFHS) is a synthetic organosilicon compound of the form CH3O(CF3CF2CF2CF2CF2CF2CF2CF2)SiH. It is a colorless, volatile liquid with a low vapor pressure. TMFHS has a wide range of applications in organic synthesis, materials science, and biomedical research. It has been used as a precursor for the synthesis of polysilanes and other organosilicon polymers, as a reagent for the preparation of polyfluoroalkylated compounds, and as a surfactant to improve the solubility of drug molecules. In addition, it has been used as a catalyst for the hydrolysis of esters, as a reagent for the preparation of polyfluoroalkylated compounds, and as a surfactant to improve the solubility of drug molecules.
 

Scientific Research Applications

Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane has been used in a variety of scientific research applications, including materials science, organic synthesis, and biomedical research. In materials science, Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane has been used as a precursor for the synthesis of polysilanes and other organosilicon polymers. In organic synthesis, it has been used as a reagent for the preparation of polyfluoroalkylated compounds. In biomedical research, Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane has been used as a surfactant to improve the solubility of drug molecules, as a catalyst for the hydrolysis of esters, and as a reagent for the preparation of polyfluoroalkylated compounds.
 

Mechanism of Action

The mechanism of action of Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane is not fully understood. However, it is believed that the fluorinated alcohols in the fluorination reaction act as a Lewis acid, while the TMS precursor functions as a Lewis base. This reaction results in the formation of a complex between the TMS precursor and the fluorinated alcohols, which then undergoes a nucleophilic substitution reaction to form the desired product, Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane.
 

Biochemical and Physiological Effects

The biochemical and physiological effects of Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane have not been thoroughly studied. However, studies have shown that Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane can act as a surfactant, increasing the solubility of drug molecules in aqueous solutions. It has also been shown to act as a catalyst for the hydrolysis of esters, and as a reagent for the preparation of polyfluoroalkylated compounds.
 

Advantages and Limitations for Lab Experiments

Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane has several advantages for use in laboratory experiments. It has a low vapor pressure, making it easy to handle and store. It is also relatively inexpensive and has a wide range of applications in organic synthesis, materials science, and biomedical research. However, there are some potential limitations to its use. It is a volatile liquid, so it must be handled with care. In addition, it is flammable and should not be used near open flames.
 

Future Directions

The potential applications of Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane are still being explored. Future research should focus on developing new methods for the synthesis of Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane and its derivatives, as well as exploring its potential applications in other areas such as drug delivery and nanotechnology. Additionally, further studies should be conducted to better understand the biochemical and physiological effects of Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane. Finally, research should be conducted to explore the potential toxicity of Trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane and its derivatives.

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