4-(benzyloxy)-3-fluorophenylboronic acid

98%

Reagent Code: #90735
label
Alias 4-Benzyloxy-3-fluorophenylboronic acid
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CAS Number 133057-83-7

science Other reagents with same CAS 133057-83-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.04 g/mol
Formula C₁₃H₁₂BFO₃
badge Registry Numbers
MDL Number MFCD00994627
thermostat Physical Properties
Melting Point 116 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, it is used in material science for designing advanced polymers and functional materials. Its boronic acid group allows for selective binding to diols, making it useful in sensor development for detecting sugars and other analytes.

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Test Parameter Specification
Purity (LC) 98-100
Appearance White to off-white powder
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿380.00
inventory 1g
10-20 days ฿850.00
inventory 5g
10-20 days ฿2,580.00

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4-(benzyloxy)-3-fluorophenylboronic acid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, it is used in material science for designing advanced poly

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the development of drug candidates by facilitating the synthesis of biologically active compounds. Additionally, it is used in material science for designing advanced polymers and functional materials. Its boronic acid group allows for selective binding to diols, making it useful in sensor development for detecting sugars and other analytes.

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