Silver trifluoromethanesulfonate

97%

Reagent Code: #234396
label
Alias Silver trifluoromethanesulfonate (Ⅰ)
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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

description Product Description

Used as a catalyst in organic synthesis, particularly in reactions involving glycosylation and alkylation due to its strong Lewis acidity. It promotes coupling reactions and is effective in activating carbon-carbon and carbon-heteroatom bond formations. Commonly employed in the preparation of pharmaceuticals and fine chemicals where high selectivity and yield are required. Also utilized in electrochemical applications and as a reagent in the synthesis of other triflate salts. Its stability under various reaction conditions makes it suitable for use in both laboratory and industrial settings.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿750.00
inventory 10g
10-20 days ฿1,360.00
inventory 25g
10-20 days ฿3,150.00
inventory 100g
10-20 days ฿11,800.00

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Silver trifluoromethanesulfonate
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Used as a catalyst in organic synthesis, particularly in reactions involving glycosylation and alkylation due to its strong Lewis acidity. It promotes coupling reactions and is effective in activating carbon-carbon and carbon-heteroatom bond formations. Commonly employed in the preparation of pharmaceuticals and fine chemicals where high selectivity and yield are required. Also utilized in electrochemical applications and as a reagent in the synthesis of other triflate salts. Its stability under various

Used as a catalyst in organic synthesis, particularly in reactions involving glycosylation and alkylation due to its strong Lewis acidity. It promotes coupling reactions and is effective in activating carbon-carbon and carbon-heteroatom bond formations. Commonly employed in the preparation of pharmaceuticals and fine chemicals where high selectivity and yield are required. Also utilized in electrochemical applications and as a reagent in the synthesis of other triflate salts. Its stability under various reaction conditions makes it suitable for use in both laboratory and industrial settings.

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