5-Cyano-2-fluorophenylboronic acid
97%
- Product Code: 90927
Alias:
5-Nitrino-2-fluorophenylboronic acid
CAS:
468718-30-1
| Molecular Weight: | 164.93 g./mol | Molecular Formula: | C₇H₅BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 300 | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex biaryl structures. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for developing active ingredients. The presence of both cyano and fluoro groups enhances its reactivity and selectivity, allowing for the creation of diverse chemical scaffolds. Additionally, it is employed in the preparation of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to introduce specific functional groups into molecular frameworks. Its utility in medicinal chemistry is notable, as it aids in the synthesis of potential drug candidates targeting various diseases.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 97-100 |
| APPEARANCE | White to off-white powder |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿300.00 |
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| 1.000 | 10-20 days | ฿900.00 |
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| 5.000 | 10-20 days | ฿4,420.00 |
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5-Cyano-2-fluorophenylboronic acid
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex biaryl structures. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for developing active ingredients. The presence of both cyano and fluoro groups enhances its reactivity and selectivity, allowing for the creation of diverse chemical scaffolds. Additionally, it is employed in the preparation of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to introduce specific functional groups into molecular frameworks. Its utility in medicinal chemistry is notable, as it aids in the synthesis of potential drug candidates targeting various diseases.
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