Potassium trifluoro(4-fluoro-2-methylbenzyl)borate

95%

Reagent Code: #131215
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CAS Number 2828444-52-4

science Other reagents with same CAS 2828444-52-4

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Weight 229.05 g/mol
Formula C₈H₇BF₄K
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MDL Number MFCD30286931
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions where selective boron-based intermediates are required. Its structure enables enhanced stability and reactivity in the formation of carbon-carbon bonds, especially in the development of pharmaceuticals and agrochemicals. The fluorinated benzyl group improves lipophilicity and metabolic stability in drug design, making this compound valuable in late-stage functionalization of complex molecules. It is also employed in the preparation of boron-containing probes for medicinal chemistry and imaging applications.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,560.00
inventory 250mg
10-20 days ฿23,410.00

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Potassium trifluoro(4-fluoro-2-methylbenzyl)borate
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Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions where selective boron-based intermediates are required. Its structure enables enhanced stability and reactivity in the formation of carbon-carbon bonds, especially in the development of pharmaceuticals and agrochemicals. The fluorinated benzyl group improves lipophilicity and metabolic stability in drug design, making this compound valuable in late-stage functionalization of complex molecules. It is also employed

Used as a specialized reagent in organic synthesis, particularly in cross-coupling reactions where selective boron-based intermediates are required. Its structure enables enhanced stability and reactivity in the formation of carbon-carbon bonds, especially in the development of pharmaceuticals and agrochemicals. The fluorinated benzyl group improves lipophilicity and metabolic stability in drug design, making this compound valuable in late-stage functionalization of complex molecules. It is also employed in the preparation of boron-containing probes for medicinal chemistry and imaging applications.

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