Dibenzo[b,d]iodol-5-ium trifluoromethanesulfonate

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Reagent Code: #167331
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CAS Number 189999-35-7

science Other reagents with same CAS 189999-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 428.17 g/mol
Formula C₁₃H₈F₃IO₃S
badge Registry Numbers
MDL Number MFCD30541552
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Widely used as a highly efficient arylating agent in organic synthesis, particularly in the construction of biaryl frameworks through metal-free C–H functionalization. It enables the direct coupling of arenes under mild conditions, making it valuable in pharmaceutical and agrochemical research where complex aromatic systems are common. Its triflate counterion enhances solubility and reactivity in polar organic solvents, facilitating reactions such as aryl transfer to heteroarenes and electron-rich aromatics. Due to its stability and selectivity, it is favored in late-stage functionalization of bioactive molecules, allowing for rapid diversification without the need for transition metal catalysts.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20,540.00
inventory 5g
10-20 days ฿71,870.00

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Dibenzo[b,d]iodol-5-ium trifluoromethanesulfonate
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Widely used as a highly efficient arylating agent in organic synthesis, particularly in the construction of biaryl frameworks through metal-free C–H functionalization. It enables the direct coupling of arenes under mild conditions, making it valuable in pharmaceutical and agrochemical research where complex aromatic systems are common. Its triflate counterion enhances solubility and reactivity in polar organic solvents, facilitating reactions such as aryl transfer to heteroarenes and electron-rich aromat

Widely used as a highly efficient arylating agent in organic synthesis, particularly in the construction of biaryl frameworks through metal-free C–H functionalization. It enables the direct coupling of arenes under mild conditions, making it valuable in pharmaceutical and agrochemical research where complex aromatic systems are common. Its triflate counterion enhances solubility and reactivity in polar organic solvents, facilitating reactions such as aryl transfer to heteroarenes and electron-rich aromatics. Due to its stability and selectivity, it is favored in late-stage functionalization of bioactive molecules, allowing for rapid diversification without the need for transition metal catalysts.

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