N-Phenylbis(trifluoromethanesulphonimide) CAS: 37595-74-7
Catalog Number | XD95214 |
Product Name | N-Phenylbis(trifluoromethanesulphonimide) |
CAS | 37595-74-7 |
Molecular Formula | C8H5F6NO4S2 |
Molecular Weight | 357.25 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
N-Phenylbis(trifluoromethanesulfonylimide), also known as PhNTf2, is a chemical compound with various applications in different industries. Its unique properties and reactivity make it valuable in several areas.
In the field of organic synthesis, PhNTf2 is used as a strong acid catalyst and a versatile reagent for various transformations. It can activate various functional groups, such as alkenes, alkynes, and carbonyl compounds, to undergo a wide range of reactions, including Friedel-Crafts reactions, acylation reactions, and rearrangement reactions. This compound's catalytic activity allows for the efficient and selective formation of complex organic molecules.
Furthermore, PhNTf2 finds applications in the field of electrochemistry as an electrolyte additive in batteries and supercapacitors. Its high ionic conductivity and stability make it suitable for improving the performance and efficiency of these energy storage devices. This compound can enhance the charge/discharge kinetics, increase the cycling stability, and improve the overall energy storage capabilities.
In the field of materials science, PhNTf2 can be used as a dopant or an additive to modify the properties of materials. It can enhance the conductivity, stability, and electrochemical performance of polymers, composites, and other functional materials. This compound's ability to form stable complexes with metal ions makes it useful in various applications, such as catalysis, sensing, and energy storage.
Additionally, PhNTf2 has applications in the field of pharmaceuticals and agrochemicals. It can be used as a building block or a protecting group in the synthesis of bioactive compounds. Its unique combination of phenyl and trifluoromethanesulfonylimide groups allows for the modification of the molecular structure, leading to improved bioactivity, stability, or solubility.
In conclusion, N-Phenylbis(trifluoromethanesulfonylimide) has diverse applications in organic synthesis, electrochemistry, materials science, and pharmaceuticals. Its catalytic activity, electrolyte properties, and modification capabilities make it valuable in these fields. Continued research and development are expanding the potential applications of this compound in various industries.