2,3-Difluorophenylboronic acid
97%
- Product Code: 89546
Alias:
2,3-Difluorophenylboronic acid
CAS:
121219-16-7
| Molecular Weight: | 157.91 g./mol | Molecular Formula: | C₆H₅BF₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01863170 | |
| Melting Point: | 95 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
2,3-Difluorophenylboronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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 boronic acid group facilitates the coupling with aryl halides or vinyl halides, enabling the creation of diverse chemical structures. Additionally, it is utilized in the development of sensors and catalysts due to its ability to interact with diols and other functional groups. Its applications extend to research and development in medicinal chemistry, where it aids in the design and synthesis of potential drug candidates.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5-100 |
| APPEARANCE | Off-white powder |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $17.85 |
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| 5.000 | 10-20 days | $38.98 |
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| 25.000 | 10-20 days | $157.80 |
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| 100.000 | 10-20 days | $498.76 |
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2,3-Difluorophenylboronic acid
2,3-Difluorophenylboronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form 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 boronic acid group facilitates the coupling with aryl halides or vinyl halides, enabling the creation of diverse chemical structures. Additionally, it is utilized in the development of sensors and catalysts due to its ability to interact with diols and other functional groups. Its applications extend to research and development in medicinal chemistry, where it aids in the design and synthesis of potential drug candidates.
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