Silver trifluoromethanesulfonate

99.9%, water≤0.2%

Reagent Code: #233705
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CAS Number 2923-28-6

science Other reagents with same CAS 2923-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.94 g/mol
Formula CF₃SO₃Ag
badge Registry Numbers
EC Number 220-882-2
MDL Number MFCD00013226
thermostat Physical Properties
Melting Point 286 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a catalyst in organic synthesis, particularly in reactions involving alkylation and acylation due to its strong Lewis acidity. It promotes carbon-carbon and carbon-heteroatom bond formations efficiently. Commonly employed in glycosylation reactions for carbohydrate chemistry, enabling the synthesis of complex sugars. Also utilized in halogenation processes where it activates halogen sources selectively. Its high solubility in polar organic solvents makes it suitable for homogeneous catalytic systems. Additionally, it serves as a reagent in the preparation of other triflate salts and in electrochemical applications due to its ionic conductivity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,470.00
inventory 25g
10-20 days ฿6,000.00
inventory 100g
10-20 days ฿19,880.00
inventory 500g
10-20 days ฿90,780.00

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Silver trifluoromethanesulfonate
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Used as a catalyst in organic synthesis, particularly in reactions involving alkylation and acylation due to its strong Lewis acidity. It promotes carbon-carbon and carbon-heteroatom bond formations efficiently. Commonly employed in glycosylation reactions for carbohydrate chemistry, enabling the synthesis of complex sugars. Also utilized in halogenation processes where it activates halogen sources selectively. Its high solubility in polar organic solvents makes it suitable for homogeneous catalytic syst

Used as a catalyst in organic synthesis, particularly in reactions involving alkylation and acylation due to its strong Lewis acidity. It promotes carbon-carbon and carbon-heteroatom bond formations efficiently. Commonly employed in glycosylation reactions for carbohydrate chemistry, enabling the synthesis of complex sugars. Also utilized in halogenation processes where it activates halogen sources selectively. Its high solubility in polar organic solvents makes it suitable for homogeneous catalytic systems. Additionally, it serves as a reagent in the preparation of other triflate salts and in electrochemical applications due to its ionic conductivity.

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