Phenyl-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]iodonium trifluoromethanesulfonate is a specialized organoiodine compound known for its unique reactivity and stability. This substance features a phenyl group attached to a tetrafluoroethyl moiety, which is further substituted with a trifluoromethyl group, enhancing its electrophilic character. The presence of the iodonium ion contributes to its utility in various chemical reactions, particularly in electrophilic aromatic substitutions and as a reagent in organic synthesis. The trifluoromethanesulfonate counterion is known for its excellent leaving group properties, facilitating nucleophilic attacks. This compound is typically used in advanced materials science and organic synthesis, where its high reactivity can be harnessed for the formation of complex molecular architectures. Additionally, the fluorinated groups impart unique physical properties, such as increased thermal stability and solubility in nonpolar solvents. Safety precautions are essential when handling this compound due to its potential reactivity and the toxicity associated with some of its components.

phenyl-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]iodonium; trifluoromethanesulfonate

82959-18-0: Phenyl-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]iodonium trifluoromethanesulfonate is a specialized organoiodine compound known for its unique reactivity and stability. This substance features a phenyl group attached to a tetrafluoroethyl moiety, which is further substituted with a trifluoromethyl group, enhancing its electrophilic character. The presence of the iodonium ion contributes to its utility in various chemical reactions, particularly in electrophilic aromatic substitutions and as a reagent in organic synthesis. The trifluoromethanesulfonate counterion is known for its excellent leaving group properties, facilitating nucleophilic attacks. This compound is typically used in advanced materials science and organic synthesis, where its high reactivity can be harnessed for the formation of complex molecular architectures. Additionally, the fluorinated groups impart unique physical properties, such as increased thermal stability and solubility in nonpolar solvents. Safety precautions are essential when handling this compound due to its potential reactivity and the toxicity associated with some of its components.

CAS 82959-18-0

phenyl-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]iodonium; trifluoromethanesulfonate

(PERFLUOROISOPROPYL)PHENYLIODONIUM TRIFLUOROMETHANESULFONATE

Ref: IN-DA003C1R