Trifluoromethanesulfonylchloride CAS:421-83-0
Catalog Number | XD96325 |
Product Name | Trifluoromethanesulfonylchloride |
CAS | 421-83-0 |
Molecular Formula | CClF3O2S |
Molecular Weight | 168.52 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
Trifluoromethanesulfonyl chloride, also known as triflyl chloride or TfCl, is a highly reactive chemical compound with several notable effects and applications in organic chemistry.One of the primary effects of trifluoromethanesulfonyl chloride is its ability to serve as a powerful electrophile. The sulfonic acid chloride moiety (-SO2Cl) makes it highly reactive towards nucleophiles, allowing it to participate in a wide range of chemical reactions. It is commonly used as a reagent for the introduction of the triflyl group (-SO2CF3) into organic molecules.The triflyl group is a versatile functional group that possesses unique properties. It is an effective leaving group in nucleophilic substitution reactions and can be easily replaced by various nucleophiles, such as amines, alcohols, and thiols. Trifluoromethanesulfonyl chloride has been widely utilized in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals due to the desirable effects conferred by the triflyl group on the resulting compounds.In addition to its electrophilic properties, trifluoromethanesulfonyl chloride also serves as a useful protecting group in organic synthesis. It can be used to protect various functional groups, such as alcohols and amines, by forming stable and easily cleavable sulfonate esters. This temporary protection allows specific reactions to be carried out with other functional groups in the molecule, and the triflyl group can be subsequently removed under mild conditions to regenerate the original functional group.Moreover, trifluoromethanesulfonyl chloride has been employed in a range of organic transformations, including rearrangements, carbonyl activation reactions, and functional group conversions. Its reactivity and ability to participate in a variety of reactions make it a valuable tool in the synthesis of complex organic molecules.It is worth noting that trifluoromethanesulfonyl chloride is a highly toxic and corrosive compound and should be handled with extreme caution. Proper safety measures should be followed, such as working in a well-ventilated area and wearing appropriate protective equipment.In summary, trifluoromethanesulfonyl chloride is a reactive compound with multiple effects and applications in organic chemistry. It serves as a powerful electrophile and can introduce the triflyl group into organic molecules, offering unique properties and increasing the value of resulting compounds. It is also used as a protecting group and participates in various organic transformations. However, its toxicity and corrosiveness should be respected, and safety precautions should be taken when handling trifluoromethanesulfonyl chloride.