4-Fluorophenylboronic acid

98%

Reagent Code: #90611
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Alias 4-fluorophenylboronic acid; p-fluorophenylboronic acid
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CAS Number 1765-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.92 g/mol
Formula C₆H₆BFO₂
badge Registry Numbers
MDL Number MFCD00039136
thermostat Physical Properties
Melting Point 262-265 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

4-Fluorophenylboronic 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 acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its fluorophenyl group enhances the stability and reactivity of the boronic acid, making it a preferred choice in various catalytic processes. Additionally, it is utilized in the development of sensors and diagnostic reagents due to its ability to interact selectively with specific biological targets.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 97.5-100%
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿14,300.00
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿390.00
inventory 25g
10-20 days ฿910.00
inventory 100g
10-20 days ฿2,980.00
4-Fluorophenylboronic acid
4-Fluorophenylboronic 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 acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its fluorophenyl group enhances the stability and reactivity of the boronic acid, making it a preferred choice in various catalytic processes. Additionally, it is utilized in the development of sensors and diagnostic reagents due to its ability to interact selectively with specific biological targets.
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