potassium trifluoro(3-fluoro-4-methoxyphenyl)borate(1-)

98%

Reagent Code: #226147
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CAS Number 850623-62-0

science Other reagents with same CAS 850623-62-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.0249 g/mol
Formula C₇H₆BF₄KO
badge Registry Numbers
MDL Number MFCD04115757
thermostat Physical Properties
Melting Point 276-280℃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions involving aryl fluorides. Its unique structure enhances reactivity and selectivity in forming carbon-carbon bonds, especially in pharmaceutical and agrochemical manufacturing. It serves as a source of trifluoroborate species in metal-catalyzed transformations, offering improved stability and solubility compared to other boron reagents. Commonly applied in the synthesis of complex fluorinated molecules where precise control over regiochemistry is required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿580.00
inventory 1g
10-20 days ฿1,550.00
inventory 5g
10-20 days ฿5,440.00
potassium trifluoro(3-fluoro-4-methoxyphenyl)borate(1-)
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Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions involving aryl fluorides. Its unique structure enhances reactivity and selectivity in forming carbon-carbon bonds, especially in pharmaceutical and agrochemical manufacturing. It serves as a source of trifluoroborate species in metal-catalyzed transformations, offering improved stability and solubility compared to other boron reagents. Commonly applied in the synthesis of complex fluorinated molecules where preci

Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions involving aryl fluorides. Its unique structure enhances reactivity and selectivity in forming carbon-carbon bonds, especially in pharmaceutical and agrochemical manufacturing. It serves as a source of trifluoroborate species in metal-catalyzed transformations, offering improved stability and solubility compared to other boron reagents. Commonly applied in the synthesis of complex fluorinated molecules where precise control over regiochemistry is required.

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