2-Fluoro-5-(methoxycarbonyl)pyridine-3-boronic acid
95%
- Product Code: 91634
CAS:
2225175-76-6
| Molecular Weight: | 198.9441832 g./mol | Molecular Formula: | C₇H₇BFNO₄ |
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| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile boronic acid derivative, enabling the formation of carbon-carbon bonds with aryl or vinyl halides. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its pyridine ring structure and functional groups allow for precise modifications in drug design, contributing to the development of bioactive compounds. Additionally, its fluorine substituent can enhance the stability and reactivity of the molecule in various chemical transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,520.00 |
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| 0.025 | 10-20 days | ฿45,060.00 |
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| 0.100 | 10-20 days | ฿135,200.00 |
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2-Fluoro-5-(methoxycarbonyl)pyridine-3-boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile boronic acid derivative, enabling the formation of carbon-carbon bonds with aryl or vinyl halides. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its pyridine ring structure and functional groups allow for precise modifications in drug design, contributing to the development of bioactive compounds. Additionally, its fluorine substituent can enhance the stability and reactivity of the molecule in various chemical transformations.
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