(2-fluoro-6-morpholinopyridin-3-yl)boronic acid
95%
- Product Code: 67389
CAS:
955374-17-1
| Molecular Weight: | 226.0125832 g./mol | Molecular Formula: | C₉H₁₂BFN₂O₃ |
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| EC Number: | MDL Number: | MFCD18261461 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures, which are common in many drug molecules. Additionally, its morpholine and fluorine substituents contribute to its potential in designing compounds with enhanced biological activity and improved pharmacokinetic properties. It is also explored in material science for the development of organic electronic materials due to its ability to form stable conjugated systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,535.00 |
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| 0.250 | 10-20 days | ฿21,780.00 |
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(2-fluoro-6-morpholinopyridin-3-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures, which are common in many drug molecules. Additionally, its morpholine and fluorine substituents contribute to its potential in designing compounds with enhanced biological activity and improved pharmacokinetic properties. It is also explored in material science for the development of organic electronic materials due to its ability to form stable conjugated systems.
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