2-Methoxycarbonyl-5-fluorophenylboronic acid
98%
- Product Code: 48540
CAS:
850568-05-7
| Molecular Weight: | 197.9561 g./mol | Molecular Formula: | C₈H₈BFO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03095367 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its methoxycarbonyl and fluorine substituents enhance its reactivity and selectivity, allowing for the synthesis of fluorinated compounds, which are often sought after in drug development due to their improved metabolic stability and bioavailability. Its applications extend to the creation of bioactive molecules and functional materials in research and industrial settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $65.54 |
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2-Methoxycarbonyl-5-fluorophenylboronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its methoxycarbonyl and fluorine substituents enhance its reactivity and selectivity, allowing for the synthesis of fluorinated compounds, which are often sought after in drug development due to their improved metabolic stability and bioavailability. Its applications extend to the creation of bioactive molecules and functional materials in research and industrial settings.
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