2-Fluoro-6-(2-thienyl)pyridine-3-boronic acid
95%
- Product Code: 91641
CAS:
2225178-20-9
| Molecular Weight: | 223.0317832 g./mol | Molecular Formula: | C₉H₇BFNO₂S |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl structures. Additionally, its thienyl and pyridine moieties contribute to its application in materials science, where it can be incorporated into organic electronic materials or coordination polymers. Its fluorine substituent further enhances its reactivity and potential use in designing bioactive compounds with improved metabolic stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,982.00 |
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| 0.025 | 10-20 days | ฿29,700.00 |
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| 0.100 | 10-20 days | ฿82,800.00 |
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2-Fluoro-6-(2-thienyl)pyridine-3-boronic acid
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for creating complex organic molecules, often used in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl structures. Additionally, its thienyl and pyridine moieties contribute to its application in materials science, where it can be incorporated into organic electronic materials or coordination polymers. Its fluorine substituent further enhances its reactivity and potential use in designing bioactive compounds with improved metabolic stability.
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