Potassium trifluoro(2-fluoro-6-methylpyridin-3-yl)borate

98%

Reagent Code: #227854
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CAS Number 1098173-30-8

science Other reagents with same CAS 1098173-30-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.01 g/mol
Formula C₆H₅BF₄KN
badge Registry Numbers
MDL Number MFCD09260453
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Particularly effective in constructing biaryl frameworks found in active pharmaceutical ingredients. Its fluorinated pyridyl structure enhances stability and reactivity with aryl halides under mild conditions, making it suitable for late-stage functionalization in drug development. Commonly applied in the preparation of kinase inhibitors and other nitrogen-containing heterocyclic compounds in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,110.00
inventory 1g
10-20 days ฿11,700.00
inventory 5g
10-20 days ฿54,590.00
Potassium trifluoro(2-fluoro-6-methylpyridin-3-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 pharmaceutical synthesis. Particularly effective in constructing biaryl frameworks found in active pharmaceutical ingredients. Its fluorinated pyridyl structure enhances stability and reactivity with aryl halides under mild conditions, making it suitable for late-stage functionalization in drug development. Commonly applied in the preparation of kinase inhibitors and other nitrogen-containin

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Particularly effective in constructing biaryl frameworks found in active pharmaceutical ingredients. Its fluorinated pyridyl structure enhances stability and reactivity with aryl halides under mild conditions, making it suitable for late-stage functionalization in drug development. Commonly applied in the preparation of kinase inhibitors and other nitrogen-containing heterocyclic compounds in medicinal chemistry.

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