Copper(I) Trifluoromethanesulfonate

95%

Reagent Code: #173437
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CAS Number 42152-44-3

science Other reagents with same CAS 42152-44-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.62 g/mol
Formula CF₃O₃SCu
badge Registry Numbers
MDL Number MFCD18071026
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used as a catalyst in organic synthesis, particularly in coupling reactions such as C–N, C–O, and C–S bond formations. It is effective in facilitating the formation of carbon-heteroatom bonds under mild conditions, making it valuable in pharmaceutical and fine chemical manufacturing. Its high reactivity and stability allow for efficient transformations in the synthesis of complex molecules, including drug intermediates and functional materials. Also employed in click chemistry, especially in azide-alkyne cycloaddition reactions, where it acts as a source of copper(I) to promote regioselective triazole formation.

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Test Parameter Specification
Appearance Purple to red to gray solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿168.00
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿1,090.00
inventory 25g
10-20 days ฿3,980.00
inventory 100g
10-20 days ฿15,770.00

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Copper(I) Trifluoromethanesulfonate
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Widely used as a catalyst in organic synthesis, particularly in coupling reactions such as C–N, C–O, and C–S bond formations. It is effective in facilitating the formation of carbon-heteroatom bonds under mild conditions, making it valuable in pharmaceutical and fine chemical manufacturing. Its high reactivity and stability allow for efficient transformations in the synthesis of complex molecules, including drug intermediates and functional materials. Also employed in click chemistry, especially in azide-al
Widely used as a catalyst in organic synthesis, particularly in coupling reactions such as C–N, C–O, and C–S bond formations. It is effective in facilitating the formation of carbon-heteroatom bonds under mild conditions, making it valuable in pharmaceutical and fine chemical manufacturing. Its high reactivity and stability allow for efficient transformations in the synthesis of complex molecules, including drug intermediates and functional materials. Also employed in click chemistry, especially in azide-alkyne cycloaddition reactions, where it acts as a source of copper(I) to promote regioselective triazole formation.
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