(2-Fluoro-4-(methylcarbamoyl)phenyl)boronic acid
98%
- Product Code: 67388
CAS:
874289-23-3
| Molecular Weight: | 196.98 g./mol | Molecular Formula: | C₈H₉BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11856043 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to facilitate the introduction of specific functional groups into target molecules. Additionally, it finds use in material science for the synthesis of advanced polymers and other functional materials. Its fluoro and carbamoyl substituents further enhance its reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿15,420.00 |
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(2-Fluoro-4-(methylcarbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to facilitate the introduction of specific functional groups into target molecules. Additionally, it finds use in material science for the synthesis of advanced polymers and other functional materials. Its fluoro and carbamoyl substituents further enhance its reactivity and selectivity in various chemical transformations.
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