Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 147531-11-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Diphenyl(trifluoromethyl)sulfonium trifluoromethanesulfonate delivers a potent electrophilic trifluoromethyl source under mild conditions. This bench-stable sulfonium salt features a highly reactive trifluoromethyl group flanked by two aryl moieties, enabling efficient C–CF₃ bond formation in organic synthesis. Its moisture-tolerant nature simplifies handling, while the triflate counterion enhances solubility and reactivity across diverse reaction media.
Diphenyl(trifluoromethyl)sulfonium trifluoromethanesulfonate serves as a highly effective trifluoromethylating agent in organic synthesis, enabling direct C–H trifluoromethylation under mild conditions. Its bench-stable nature and compatibility with diverse functional groups facilitate efficient incorporation of the CF₃ moiety into aromatic and heteroaromatic systems. The reagent functions reliably in transition-metal-free transformations and is particularly valuable for constructing CF₃-containing scaffolds relevant to pharmaceutical and agrochemical development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P301+P310-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: