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 |
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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 |
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Purity | 97-100 |
APPEARANCE | WHITE TO LIGHT YELLOW POWDER OR CRYSTALS |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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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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