CAS 67497-95-4
:Ethanesulfonamide, 2,2,2-trifluoro-
Description:
Ethanesulfonamide, 2,2,2-trifluoro- is a chemical compound characterized by the presence of a sulfonamide functional group attached to an ethane backbone, with three fluorine atoms substituted at the second carbon. This structure imparts unique properties to the compound, including increased polarity and potential reactivity due to the electronegative fluorine atoms. The trifluoromethyl group can enhance the compound's lipophilicity, affecting its solubility and interaction with biological systems. Ethanesulfonamide derivatives are often studied for their potential applications in pharmaceuticals, particularly as antimicrobial agents or in other therapeutic contexts. The presence of the sulfonamide group suggests that it may exhibit properties similar to other sulfonamide drugs, such as antibacterial activity. Additionally, the trifluoromethyl group can influence the compound's pharmacokinetics and pharmacodynamics. Safety and handling considerations are essential, as with many fluorinated compounds, due to potential toxicity and environmental impact. Overall, Ethanesulfonamide, 2,2,2-trifluoro- represents a compound of interest in both synthetic chemistry and medicinal applications.
Formula:C2H4F3NO2S
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Found 2 products.
2,2,2-Trifluoroethanesulfonamide
CAS:<p>2,2,2-Trifluoroethanesulfonamide is an activating agent that binds to the estrogen receptor α and inhibits histone deacetylase. It is used as a chemotherapeutic drug for breast cancer. 2,2,2-Trifluoroethanesulfonamide has been shown to inhibit the growth of MCF-7 cells by reducing glutamate uptake and fatty acid synthesis. This agent also reduces the production of l-glutamic acid in these cells, which may be related to its ability to inhibit leukemia cell proliferation.</p>Formula:C2H4F3NO2SPurity:Min. 95%Molecular weight:163.12 g/mol
