4-Fluoro-3-methoxybenzeneboronic acid

97%

Reagent Code: #90605
label
Alias 4-fluoro-3-methoxyphenylboronic acid
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CAS Number 854778-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.95 g/mol
Formula C₇H₈BFO₃
badge Registry Numbers
MDL Number MFCD08056358
thermostat Physical Properties
Melting Point 189-191
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

4-Fluoro-3-methoxybenzeneboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key building block in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient coupling with aryl halides, while the fluorine and methoxy substituents can influence the reactivity and stability of the resulting products. Additionally, it is utilized in the development of sensors and catalysts due to its unique electronic properties.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 189-191
Purity (HPLC) 97-100%
Appearance White to off-white powder, solid, or chunks
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿11,820.00
inventory 250mg
10-20 days ฿330.00
inventory 1g
10-20 days ฿610.00
inventory 5g
10-20 days ฿2,820.00
4-Fluoro-3-methoxybenzeneboronic acid
4-Fluoro-3-methoxybenzeneboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key building block in the synthesis of complex organic molecules, including drug candidates and biologically active compounds. Its boronic acid group enables efficient coupling with aryl halides, while the fluorine and methoxy substituents can influence the reactivity and stability of the resulting products. Additionally, it is utilized in the development of sensors and catalysts due to its unique electronic properties.
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