(4-Cyanophenyl)(mesityl)iodonium trifluoromethanesulfonate

97%

Reagent Code: #129827
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CAS Number 1416277-02-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 497.27 g/mol
Formula C₁₇H₁₅F₃INO₃S
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 in photoredox catalysis and radical reactions. It serves as a source of aryl radicals under mild conditions, enabling the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in late-stage functionalization of complex molecules, including pharmaceuticals and agrochemicals, due to its stability and selectivity. Also utilized in materials science for the synthesis of conjugated organic systems and functionalized aromatic compounds. Its triflate counterion enhances solubility in polar organic solvents, facilitating homogeneous reaction conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,770.00
inventory 1g
10-20 days ฿7,450.00
inventory 5g
10-20 days ฿26,050.00
(4-Cyanophenyl)(mesityl)iodonium trifluoromethanesulfonate
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Used as a highly efficient arylating agent in organic synthesis, particularly in photoredox catalysis and radical reactions. It serves as a source of aryl radicals under mild conditions, enabling the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in late-stage functionalization of complex molecules, including pharmaceuticals and agrochemicals, due to its stability and selectivity. Also utilized in materials science for the synthesis of conjugated organic systems and functionaliz

Used as a highly efficient arylating agent in organic synthesis, particularly in photoredox catalysis and radical reactions. It serves as a source of aryl radicals under mild conditions, enabling the formation of carbon–carbon and carbon–heteroatom bonds. Commonly applied in late-stage functionalization of complex molecules, including pharmaceuticals and agrochemicals, due to its stability and selectivity. Also utilized in materials science for the synthesis of conjugated organic systems and functionalized aromatic compounds. Its triflate counterion enhances solubility in polar organic solvents, facilitating homogeneous reaction conditions.

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