2,5-Difluorophenylboronic acid

97%

Reagent Code: #89576
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Alias 2,5-Difluorophenylboronic acid
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CAS Number 193353-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.91 g/mol
Formula C₆H₅BF₂O₂
badge Registry Numbers
MDL Number MFCD01863171
thermostat Physical Properties
Melting Point 105-110 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

2,5-Difluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its fluorinated phenyl group enhances the reactivity and stability of the boronic acid, making it a valuable building block in medicinal chemistry for drug discovery and development. Additionally, it is employed in the preparation of fluorescent dyes and sensors, where the fluorine atoms contribute to the desired electronic properties. Its versatility also extends to polymer chemistry, where it aids in creating functionalized polymers with specific properties.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97-100
Appearance White to light yellow powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿4,260.00
inventory 1g
10-20 days ฿480.00
inventory 5g
10-20 days ฿1,320.00
inventory 100g
10-20 days ฿13,880.00
2,5-Difluorophenylboronic acid
2,5-Difluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its fluorinated phenyl group enhances the reactivity and stability of the boronic acid, making it a valuable building block in medicinal chemistry for drug discovery and development. Additionally, it is employed in the preparation of fluorescent dyes and sensors, where the fluorine atoms contribute to the desired electronic properties. Its versatility also extends to polymer chemistry, where it aids in creating functionalized polymers with specific properties.
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