(5-Fluorobenzofuran-2-yl)boronic acid
98%
- Product Code: 89354
CAS:
473416-33-0
| Molecular Weight: | 179.94 g./mol | Molecular Formula: | C₈H₆BFO₃ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
(5-Fluorobenzofuran-2-yl)boronic acid finds significant use in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and organic materials. The compound serves as a key intermediate in the synthesis of complex molecules, especially those containing the benzofuran moiety, which is common in bioactive compounds. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the creation of diverse chemical structures. Additionally, it is utilized in the development of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its fluorine substituent further enhances its reactivity and selectivity in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿1,431.00 |
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| 0.100 | 10-20 days | ฿3,447.00 |
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(5-Fluorobenzofuran-2-yl)boronic acid
(5-Fluorobenzofuran-2-yl)boronic acid finds significant use in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and organic materials. The compound serves as a key intermediate in the synthesis of complex molecules, especially those containing the benzofuran moiety, which is common in bioactive compounds. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the creation of diverse chemical structures. Additionally, it is utilized in the development of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its fluorine substituent further enhances its reactivity and selectivity in various chemical transformations.
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