Mesityl(phenyl)iodonium trifluoromethanesulfonate

97%

Reagent Code: #213358
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CAS Number 144930-50-7

science Other reagents with same CAS 144930-50-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 472.267 g/mol
Formula C₁₆H₁₆F₃IO₃S
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a highly effective arylating agent in organic synthesis, particularly for transferring mesityl and phenyl groups under mild conditions. Commonly employed in transition-metal-free arylation reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Valuable in pharmaceutical research for constructing complex aromatic structures. Also utilized in radical chemistry, where it acts as a source of aryl radicals upon reduction or photolysis. Its triflate counterion enhances solubility and reactivity in polar solvents, making it suitable for a wide range of transformations including heterocycle functionalization and late-stage modification of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,240.00
inventory 1g
10-20 days ฿3,340.00
inventory 5g
10-20 days ฿13,620.00
Mesityl(phenyl)iodonium trifluoromethanesulfonate
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Used as a highly effective arylating agent in organic synthesis, particularly for transferring mesityl and phenyl groups under mild conditions. Commonly employed in transition-metal-free arylation reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Valuable in pharmaceutical research for constructing complex aromatic structures. Also utilized in radical chemistry, where it acts as a source of aryl radicals upon reduction or photolysis. Its triflate counterion enhances solubili

Used as a highly effective arylating agent in organic synthesis, particularly for transferring mesityl and phenyl groups under mild conditions. Commonly employed in transition-metal-free arylation reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Valuable in pharmaceutical research for constructing complex aromatic structures. Also utilized in radical chemistry, where it acts as a source of aryl radicals upon reduction or photolysis. Its triflate counterion enhances solubility and reactivity in polar solvents, making it suitable for a wide range of transformations including heterocycle functionalization and late-stage modification of bioactive molecules.

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