[4-(dimethylcarbamoyl)-3-fluorophenyl]boronic acid
98%
- Product Code: 90532
CAS:
874289-13-1
| Molecular Weight: | 211 g./mol | Molecular Formula: | C₉H₁₁BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08436060 | |
| Melting Point: | 147-149°C | Boiling Point: | 418.8°C |
| Density: | 1.28g/mL | 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 pharmaceuticals, agrochemicals, and advanced materials. The dimethylcarbamoyl and fluorine substituents enhance its reactivity and selectivity, allowing for precise modifications in complex molecular structures. It is also employed in the development of bioactive molecules and as a building block in medicinal chemistry for designing potential drug candidates. Additionally, its stability and compatibility with various reaction conditions make it a versatile reagent in research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $908.65 |
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[4-(dimethylcarbamoyl)-3-fluorophenyl]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 pharmaceuticals, agrochemicals, and advanced materials. The dimethylcarbamoyl and fluorine substituents enhance its reactivity and selectivity, allowing for precise modifications in complex molecular structures. It is also employed in the development of bioactive molecules and as a building block in medicinal chemistry for designing potential drug candidates. Additionally, its stability and compatibility with various reaction conditions make it a versatile reagent in research and industrial applications.
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