Catechol Bis(trifluoromethanesulfonate)

≥98%

Reagent Code: #122153
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CAS Number 17763-91-6

science Other reagents with same CAS 17763-91-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 374.22 g/mol
Formula C₈H₄F₆O₆S₂
badge Registry Numbers
MDL Number MFCD00274274
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Catechol bis(trifluoromethanesulfonate) is primarily used as a versatile reagent in organic synthesis, particularly in the introduction of trifluoromethanesulfonate (triflate) groups. These groups are highly reactive and serve as excellent leaving groups in substitution reactions, making the compound valuable in the formation of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise functional group transformations are required. Additionally, its role in cross-coupling reactions, such as Suzuki and Heck reactions, is significant for constructing carbon-carbon bonds in the development of fine chemicals and active pharmaceutical ingredients (APIs). The compound’s stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿891.00
inventory 1g
10-20 days ฿2,376.00

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Catechol Bis(trifluoromethanesulfonate)
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Catechol bis(trifluoromethanesulfonate) is primarily used as a versatile reagent in organic synthesis, particularly in the introduction of trifluoromethanesulfonate (triflate) groups. These groups are highly reactive and serve as excellent leaving groups in substitution reactions, making the compound valuable in the formation of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise functional group transformations are requir
Catechol bis(trifluoromethanesulfonate) is primarily used as a versatile reagent in organic synthesis, particularly in the introduction of trifluoromethanesulfonate (triflate) groups. These groups are highly reactive and serve as excellent leaving groups in substitution reactions, making the compound valuable in the formation of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise functional group transformations are required. Additionally, its role in cross-coupling reactions, such as Suzuki and Heck reactions, is significant for constructing carbon-carbon bonds in the development of fine chemicals and active pharmaceutical ingredients (APIs). The compound’s stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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