2,5-Difluorophenylboronic acid

97%

  • Product Code: 89576
  Alias:    2,5-Difluorophenylboronic acid
  CAS:    193353-34-3
Molecular Weight: 157.91 g./mol Molecular Formula: C₆H₅BF₂O₂
EC Number: MDL Number: MFCD01863171
Melting Point: 105-110 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
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.
Product Specification:
Test Specification
Purity 97-100
APPEARANCE WHITE TO LIGHT YELLOW POWDER OR CRYSTALS
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $14.40
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5.000 10-20 days $39.60
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25.000 10-20 days $127.81
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100.000 10-20 days $416.44
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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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