Potassium trifluoro(5-formylfuran-2-yl)borate

95%

Reagent Code: #227299
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CAS Number 907604-62-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.98 g/mol
Formula C₅H₃BF₃KO₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its aldehyde-functionalized furan structure allows for further derivatization, making it valuable in pharmaceutical and agrochemical research for building bioactive compounds. The potassium salt form enhances solubility in aqueous reaction media, improving coupling efficiency under mild conditions. Commonly employed in the development of fluorescent probes and functional materials due to the reactive aldehyde group that can be easily modified post-coupling.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,150.00
1g
10-20 days ฿2,850.00
Potassium trifluoro(5-formylfuran-2-yl)borate
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its aldehyde-functionalized furan structure allows for further derivatization, making it valuable in pharmaceutical and agrochemical research for building bioactive compounds. The potassium salt form enhances solubility in aqueous reaction media, improving coupling efficiency under mild conditions. Commonly employed in the development of fluorescen

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its aldehyde-functionalized furan structure allows for further derivatization, making it valuable in pharmaceutical and agrochemical research for building bioactive compounds. The potassium salt form enhances solubility in aqueous reaction media, improving coupling efficiency under mild conditions. Commonly employed in the development of fluorescent probes and functional materials due to the reactive aldehyde group that can be easily modified post-coupling.

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