2,5-Difluorophenylboronic acid
97%
Reagent
Code: #89576
Alias
2,5-Difluorophenylboronic acid
CAS Number
193353-34-3
blur_circular Chemical Specifications
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Molecular Information
Weight
157.91 g/mol
Formula
C₆H₅BF₂O₂
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Registry Numbers
MDL Number
MFCD01863171
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Physical Properties
Melting Point
105-110 °C(lit.)
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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 |
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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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