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S-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate, also known as S-(TFTB), is an organosulfur compound used in a variety of scientific research applications. It is a highly versatile compound that is used in a variety of laboratory experiments, and its structure is composed of carbon, sulfur, and fluorine atoms. ...
S-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate, also known as S-(TFTB), is an organosulfur compound used in a variety of scientific research applications. It is a highly versatile compound that is used in a variety of laboratory experiments, and its structure is composed of carbon, sulfur, and fluorine atoms. S-(TFTB) is used in a variety of applications due to its unique properties, such as its ability to act as a Lewis acid and its resistance to hydrolysis. It is also used in a variety of biochemical and physiological experiments due to its ability to act as a redox-active species.
Fluoroalkylation, including trifluoromethylation, is a significant process in the development of pharmaceuticals, agrochemicals, and functional materials due to the unique properties imparted by fluorine atoms. Recent advancements in aqueous fluoroalkylation have opened new avenues for environment-friendly and efficient synthesis methods. The use of water as a solvent or reactant in these reactions aligns with the principles of green chemistry, showcasing the potential of fluoroalkylation in sustainable organic synthesis. This method's significance lies in its ability to introduce fluorinated groups into molecules under mild and eco-friendly conditions, highlighting a key application of S-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate in facilitating these reactions (Song et al., 2018).
The development of new herbicides is crucial for agricultural productivity and pest management. Compounds derived from S-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate have been explored for their herbicidal properties, demonstrating effective control of annual weeds and safe application on rice crops. The research in this area suggests a promising route for the synthesis of novel agrochemicals that are efficient and exhibit low environmental and mammalian toxicity, contributing to safer and more sustainable agricultural practices (Hwang et al., 2005).
Addressing climate change necessitates innovative solutions for carbon capture and conversion. Research on nitrogen-doped porous polymers, potentially catalyzed or synthesized using S-(Trifluoromethyl)dibenzothiophenium tetrafluoroborate, has shown significant promise for capturing CO2 from industrial emissions. These materials offer a sustainable and cost-effective approach to mitigating CO2's environmental impact by converting it into useful fuels or chemicals, thereby contributing to the circular carbon economy (Mukhtar et al., 2020).
Product Name : | 5-(Trifluoromethyl)-5H-dibenzo[b,d]thiophen-5-ium tetrafluoroborate | ||
CAS No. : | 131880-16-5 | Molecular Weight : | 340.07 |
MDL No. : | MFCD01073545 | Purity/ Specification : | |
Molecular Formula : | C13H8BF7S | Storage : | Keep in dark place,Inert atmosphere,Room temperature |
Boiling Point : | - |
GHS Pictogram : | |||
Signal Word : | Warning | Precautionary Statements : | P261-P305+P351+P338 |
UN# : | N/A | Class : | N/A |
Hazard Statements : | H302-H315-H319-H335 | Packing Group : | N/A |