Silver trifluoroacetate

98%

Reagent Code: #234441
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Alias Silver trifluoroacetate
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CAS Number 2966-50-9

science Other reagents with same CAS 2966-50-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.88 g/mol
Formula C₂F₃O₂Ag
badge Registry Numbers
EC Number 221-004-0
MDL Number MFCD00013199
thermostat Physical Properties
Melting Point 257-260 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly in silver-mediated fluorination and trifluoromethylation reactions. It serves as a source of silver ions in catalytic systems for cross-coupling reactions, enabling the formation of carbon–fluorine and carbon–carbon bonds. Commonly applied in the preparation of fluorinated pharmaceuticals and agrochemicals due to its ability to introduce trifluoromethyl groups efficiently. Also utilized in materials science for the synthesis of fluorinated polymers and specialty coatings where thermal and chemical stability are required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿520.00
inventory 5g
10-20 days ฿930.00
inventory 25g
10-20 days ฿3,550.00
inventory 100g
10-20 days ฿13,180.00
inventory 500g
10-20 days ฿61,900.00

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Silver trifluoroacetate
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Used as a reagent in organic synthesis, particularly in silver-mediated fluorination and trifluoromethylation reactions. It serves as a source of silver ions in catalytic systems for cross-coupling reactions, enabling the formation of carbon–fluorine and carbon–carbon bonds. Commonly applied in the preparation of fluorinated pharmaceuticals and agrochemicals due to its ability to introduce trifluoromethyl groups efficiently. Also utilized in materials science for the synthesis of fluorinated polymers and

Used as a reagent in organic synthesis, particularly in silver-mediated fluorination and trifluoromethylation reactions. It serves as a source of silver ions in catalytic systems for cross-coupling reactions, enabling the formation of carbon–fluorine and carbon–carbon bonds. Commonly applied in the preparation of fluorinated pharmaceuticals and agrochemicals due to its ability to introduce trifluoromethyl groups efficiently. Also utilized in materials science for the synthesis of fluorinated polymers and specialty coatings where thermal and chemical stability are required.

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