potassium (2,4-difluorophenyl)(trifluoro)borate(1-)

98%

Reagent Code: #226180
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CAS Number 871231-41-3

science Other reagents with same CAS 871231-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.9893 g/mol
Formula C₆H₃BF₅K
badge Registry Numbers
MDL Number MFCD07784375
thermostat Physical Properties
Melting Point >300℃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling. It serves as a stable source of the 2,4-difluorophenyl group, enabling the construction of fluorinated aromatic compounds. These compounds are valuable in the pharmaceutical and agrochemical industries due to the enhanced metabolic stability and bioavailability provided by fluorine atoms. The reagent is also employed in the development of precursors for radiotracers in positron emission tomography (PET) imaging, supporting fluorine-18 labeling strategies. Its stability and selectivity make it suitable for late-stage functionalization of complex molecules.

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Test Parameter Specification
Appearance White Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,010.00
inventory 1g
10-20 days ฿2,630.00
inventory 5g
10-20 days ฿8,270.00
potassium (2,4-difluorophenyl)(trifluoro)borate(1-)
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Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling. It serves as a stable source of the 2,4-difluorophenyl group, enabling the construction of fluorinated aromatic compounds. These compounds are valuable in the pharmaceutical and agrochemical industries due to the enhanced metabolic stability and bioavailability provided by fluorine atoms. The reagent is also employed in the development of precursors for radiotracers in positron emission t

Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura coupling. It serves as a stable source of the 2,4-difluorophenyl group, enabling the construction of fluorinated aromatic compounds. These compounds are valuable in the pharmaceutical and agrochemical industries due to the enhanced metabolic stability and bioavailability provided by fluorine atoms. The reagent is also employed in the development of precursors for radiotracers in positron emission tomography (PET) imaging, supporting fluorine-18 labeling strategies. Its stability and selectivity make it suitable for late-stage functionalization of complex molecules.

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