(4-Chlorophenyl)(mesityl)iodonium trifluoromethanesulfonate

97%

Reagent Code: #131935
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CAS Number 1204518-00-2

science Other reagents with same CAS 1204518-00-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 506.7 g/mol
Formula C₁₆H₁₅ClF₃IO₃S
thermostat Physical Properties
Melting Point 132-133 °C
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a highly efficient arylating agent in organic synthesis, particularly for transferring aryl groups under mild conditions. It is effective in metal-catalyzed and metal-free reactions, enabling the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in the synthesis of complex molecules such as pharmaceuticals and functional materials due to its stability and reactivity. Also utilized in photo-induced reactions for surface modifications and polymer chemistry. Its triflate counterion enhances solubility in polar organic solvents, making it suitable for a wide range of reaction media.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,760.00
inventory 1g
10-20 days ฿4,740.00
inventory 5g
10-20 days ฿17,950.00
(4-Chlorophenyl)(mesityl)iodonium trifluoromethanesulfonate
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Used as a highly efficient arylating agent in organic synthesis, particularly for transferring aryl groups under mild conditions. It is effective in metal-catalyzed and metal-free reactions, enabling the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in the synthesis of complex molecules such as pharmaceuticals and functional materials due to its stability and reactivity. Also utilized in photo-induced reactions for surface modifications and polymer chemistry. Its triflate count

Used as a highly efficient arylating agent in organic synthesis, particularly for transferring aryl groups under mild conditions. It is effective in metal-catalyzed and metal-free reactions, enabling the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in the synthesis of complex molecules such as pharmaceuticals and functional materials due to its stability and reactivity. Also utilized in photo-induced reactions for surface modifications and polymer chemistry. Its triflate counterion enhances solubility in polar organic solvents, making it suitable for a wide range of reaction media.

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