(2-Cyano-6-fluorophenyl)boronic acid
95%
- Product Code: 89804
CAS:
656235-44-8
| Molecular Weight: | 164.93 g./mol | Molecular Formula: | C₇H₅BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09033623 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
(2-Cyano-6-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create complex organic molecules, including drug candidates. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are common in many active pharmaceutical ingredients.
Additionally, it serves as a building block in the development of sensors and diagnostic agents. Its unique structure allows it to interact with specific biological targets, making it useful in the design of probes for detecting various analytes in biochemical research.
In material science, this compound is explored for its potential in creating advanced polymers and coatings. Its ability to participate in cross-linking reactions makes it valuable for improving the mechanical and thermal properties of materials.
Overall, (2-Cyano-6-fluorophenyl)boronic acid is a versatile reagent with significant applications in drug discovery, biochemical research, and material development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿1,278.00 |
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| 0.250 | 10-20 days | ฿2,259.00 |
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(2-Cyano-6-fluorophenyl)boronic acid
(2-Cyano-6-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create complex organic molecules, including drug candidates. The boronic acid group facilitates the formation of carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are common in many active pharmaceutical ingredients.
Additionally, it serves as a building block in the development of sensors and diagnostic agents. Its unique structure allows it to interact with specific biological targets, making it useful in the design of probes for detecting various analytes in biochemical research.
In material science, this compound is explored for its potential in creating advanced polymers and coatings. Its ability to participate in cross-linking reactions makes it valuable for improving the mechanical and thermal properties of materials.
Overall, (2-Cyano-6-fluorophenyl)boronic acid is a versatile reagent with significant applications in drug discovery, biochemical research, and material development.
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