Copper(II) trifluoromethanesulfonate

98%

Reagent Code: #158331
label
Alias Copper trifluoromethanesulfonate (II)
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CAS Number 34946-82-2

science Other reagents with same CAS 34946-82-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.68 g/mol
Formula C₂CuF₆O₆S₂
badge Registry Numbers
EC Number 252-300-8
MDL Number MFCD00077492
thermostat Physical Properties
Melting Point ≥300 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used as a Lewis acid catalyst in organic synthesis, particularly in coupling reactions and electrophilic trifluoromethylation. Effective in promoting carbon-carbon and carbon-heteroatom bond formations under mild conditions. Commonly applied in Friedel-Crafts acylations, Diels-Alder reactions, and nitro-Mannich reactions. Also utilized in the activation of aldehydes and ketones due to its strong electrophilic character. Its triflate anion provides high solubility in polar organic solvents, enhancing catalytic efficiency. Stable and reusable in some reaction systems, making it suitable for both laboratory and industrial-scale transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿250.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿1,080.00
inventory 100g
10-20 days ฿3,940.00
inventory 500g
10-20 days ฿13,800.00

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Copper(II) trifluoromethanesulfonate
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Widely used as a Lewis acid catalyst in organic synthesis, particularly in coupling reactions and electrophilic trifluoromethylation. Effective in promoting carbon-carbon and carbon-heteroatom bond formations under mild conditions. Commonly applied in Friedel-Crafts acylations, Diels-Alder reactions, and nitro-Mannich reactions. Also utilized in the activation of aldehydes and ketones due to its strong electrophilic character. Its triflate anion provides high solubility in polar organic solvents, enhanci

Widely used as a Lewis acid catalyst in organic synthesis, particularly in coupling reactions and electrophilic trifluoromethylation. Effective in promoting carbon-carbon and carbon-heteroatom bond formations under mild conditions. Commonly applied in Friedel-Crafts acylations, Diels-Alder reactions, and nitro-Mannich reactions. Also utilized in the activation of aldehydes and ketones due to its strong electrophilic character. Its triflate anion provides high solubility in polar organic solvents, enhancing catalytic efficiency. Stable and reusable in some reaction systems, making it suitable for both laboratory and industrial-scale transformations.

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