Borate(1-), trifluoro(2-fluoro-6-hydroxyphenyl)-, potassium (1: 1)

98%

Reagent Code: #151775
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CAS Number 2252415-10-2

science Other reagents with same CAS 2252415-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.00 g/mol
Formula C₆H₄BF₄KO
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MDL Number MFCD32068467
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its stable borate-fluoride structure. Its hydroxyl and fluorinated phenyl groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex organic molecules. Also employed in materials science for developing fluorescent probes and optoelectronic materials, where the boron and fluorine atoms enhance electron transport properties. The compound’s stability and reactivity profile allow for efficient transformations under mild conditions, particularly in Suzuki-Miyaura coupling reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿590.00
inventory 1g
10-20 days ฿1,640.00
inventory 5g
10-20 days ฿5,750.00
inventory 25g
10-20 days ฿20,120.00

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Borate(1-), trifluoro(2-fluoro-6-hydroxyphenyl)-, potassium (1: 1)
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its stable borate-fluoride structure. Its hydroxyl and fluorinated phenyl groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex organic molecules. Also employed in materials science for developing fluorescent probes and optoelectronic materials, where the boron and fluorine atoms enhance electron transport properties. The compound’s stability and r

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its stable borate-fluoride structure. Its hydroxyl and fluorinated phenyl groups enable selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex organic molecules. Also employed in materials science for developing fluorescent probes and optoelectronic materials, where the boron and fluorine atoms enhance electron transport properties. The compound’s stability and reactivity profile allow for efficient transformations under mild conditions, particularly in Suzuki-Miyaura coupling reactions.

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