(4-Bromo-2,3,5,6-tetrafluorophenyl)boronic acid

95%

Reagent Code: #113292
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CAS Number 1016231-40-5

science Other reagents with same CAS 1016231-40-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.79 g/mol
Formula C₆H₂BBrF₄O₂
badge Registry Numbers
MDL Number MFCD05664311
thermostat Physical Properties
Melting Point 150-154 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for introducing the tetrafluorophenyl group into more complex molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both bromine and fluorine substituents, enhances its reactivity and selectivity in forming carbon-carbon bonds. Additionally, it is employed in the preparation of fluorinated organic compounds, which are often utilized in medicinal chemistry due to their improved metabolic stability and bioavailability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,971.00
inventory 1g
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿3,339.00

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(4-Bromo-2,3,5,6-tetrafluorophenyl)boronic acid
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for introducing the tetrafluorophenyl group into more complex molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both bromine and fluorine substituents, enhances its reactivity and selectivity in forming carbon-carbon bonds. Additionally, it is employed in

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for introducing the tetrafluorophenyl group into more complex molecules, which is valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both bromine and fluorine substituents, enhances its reactivity and selectivity in forming carbon-carbon bonds. Additionally, it is employed in the preparation of fluorinated organic compounds, which are often utilized in medicinal chemistry due to their improved metabolic stability and bioavailability.

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