4-(2,2,2-Trifluoroethoxy)phenylboronic Acid

97%

Reagent Code: #90330
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CAS Number 886536-37-4

science Other reagents with same CAS 886536-37-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.95 g/mol
Formula C₈H₈BF₃O₃
badge Registry Numbers
MDL Number MFCD09027239
thermostat Physical Properties
Melting Point 191-194°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and materials science research. Additionally, it is employed in the development of bioactive compounds and advanced materials due to its stability and reactivity. Its trifluoroethoxy group can also impart unique electronic properties to the resulting products, enhancing their functionality in specific applications.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,258.00
inventory 250mg
10-20 days ฿963.00
inventory 5g
10-20 days ฿11,250.00

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4-(2,2,2-Trifluoroethoxy)phenylboronic Acid
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and materials science research. Additionally, it is employed in the development of bioactive compounds and advanced materials due to its stabil

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and materials science research. Additionally, it is employed in the development of bioactive compounds and advanced materials due to its stability and reactivity. Its trifluoroethoxy group can also impart unique electronic properties to the resulting products, enhancing their functionality in specific applications.

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