(4-(Ethoxycarbonyl)phenyl)(mesityl)iodonium trifluoromethanesulfonate

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Reagent Code: #131962
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CAS Number 1204518-04-6

science Other reagents with same CAS 1204518-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 544.32 g/mol
Formula C₁₉H₂₀F₃IO₅S
thermostat Physical Properties
Melting Point 178-179 °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 in photoredox catalysis and radical reactions. It serves as a source of aryl radicals under mild conditions, enabling C–H arylation and functionalization of complex molecules. Commonly applied in pharmaceutical research for constructing biaryl motifs and in materials science for synthesizing conjugated organic systems. Its stability and reactivity under visible light make it valuable in modern sustainable synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,400.00
inventory 1g
10-20 days ฿3,750.00
inventory 5g
10-20 days ฿14,190.00

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(4-(Ethoxycarbonyl)phenyl)(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 C–H arylation and functionalization of complex molecules. Commonly applied in pharmaceutical research for constructing biaryl motifs and in materials science for synthesizing conjugated organic systems. Its stability and reactivity under visible light make it valuable in modern sustainable synthetic methodologie

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 C–H arylation and functionalization of complex molecules. Commonly applied in pharmaceutical research for constructing biaryl motifs and in materials science for synthesizing conjugated organic systems. Its stability and reactivity under visible light make it valuable in modern sustainable synthetic methodologies.

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