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2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl methanesulfonate is a chemical compound that belongs to the class of sulfonate esters. It has been studied for its potential pharmacological properties, although it is not commonly used in clinical practice. The drug works by modulating the activity of various receptors and enzymes, which can have diverse effects on cellular function.
Mechanism of Action
2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl methanesulfonate exerts its effects by interacting with specific receptors or enzymes in the body. The exact mechanism of action is not well understood, but it is believed to involve modulation of neurotransmitter systems, ion channels, or other signaling pathways. This modulation can have therapeutic effects in various diseases.
Indications
While 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethyl methanesulfonate has shown potential pharmacological activity in laboratory studies, it is not currently approved for clinical use. Further research is needed to determine its efficacy and safety in treating specific diseases.
| English name: | 2-[2-(2,2,2-Trifluoroethoxy)phenoxylethy methanesulfonate |
| English alias: | 2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethylmethanesulfonate;SilodosinIntermediate1;2-[2-(2,2,2-trifluoroethoxy)phenoxy]-ethanol-1-Methanesulfonate;2-(2-TRIFLUOROETHOXYPHENOXY)ETHYLMETHANESULFONATE;Ethanol,2-[2-Chemicalbook(2,2,2-trifluoroethoxy)phenoxy]-,1-Methanesulfonate;2-(2-(2,2,2-Trifluoroethoxy);2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethylmethanesulfote;2-[2-(2,2,2-Trifluoroethoxy)phenoxy]ethylmethanesulfonate(forSilodoxin) |
| CAS Number: | 160969-03-9 |
| EINECS Number: | 801-482-2 |
| Molecular formula: | C11H13O3S |
| Molecular weight: | 314.28 |
| Melting point: | 52.0 to 56.0 °C |
| Boiling point: | 396.4±42.0 °C(Predicted) |
Density: | 1.362g/cm3 |
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