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

97%

Reagent Code: #131934
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CAS Number 1416353-27-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 482.06 g/mol
Formula C₁₈H₂₀BF₄IO₂
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a highly efficient hypervalent iodine reagent in organic synthesis, particularly for electrophilic arylations. It enables the transfer of the 4-(ethoxycarbonyl)phenyl group under mild conditions, with the mesityl group serving as a non-transferring ligand, making it valuable in pharmaceutical and agrochemical research. Commonly employed in metal-free coupling reactions, it serves as an arylating agent for heteroarenes, enolates, and other nucleophiles. Its tetrafluoroborate salt enhances stability and solubility in polar solvents, supporting applications in both batch and flow chemistry. Also utilized in photoinduced reactions where it acts as a precursor for aryl radical generation, enabling C–H functionalization and late-stage modifications in complex molecule synthesis.

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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
(4-(Ethoxycarbonyl)phenyl)(mesityl)iodonium tetrafluoroborate
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Used as a highly efficient hypervalent iodine reagent in organic synthesis, particularly for electrophilic arylations. It enables the transfer of the 4-(ethoxycarbonyl)phenyl group under mild conditions, with the mesityl group serving as a non-transferring ligand, making it valuable in pharmaceutical and agrochemical research. Commonly employed in metal-free coupling reactions, it serves as an arylating agent for heteroarenes, enolates, and other nucleophiles. Its tetrafluoroborate salt enhances stabilit

Used as a highly efficient hypervalent iodine reagent in organic synthesis, particularly for electrophilic arylations. It enables the transfer of the 4-(ethoxycarbonyl)phenyl group under mild conditions, with the mesityl group serving as a non-transferring ligand, making it valuable in pharmaceutical and agrochemical research. Commonly employed in metal-free coupling reactions, it serves as an arylating agent for heteroarenes, enolates, and other nucleophiles. Its tetrafluoroborate salt enhances stability and solubility in polar solvents, supporting applications in both batch and flow chemistry. Also utilized in photoinduced reactions where it acts as a precursor for aryl radical generation, enabling C–H functionalization and late-stage modifications in complex molecule synthesis.

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