6-Fluoro-3-pyridinylboronic acid
96%
- Product Code: 90953
Alias:
6-fluoropyridine-3-boronic acid
CAS:
351019-18-6
| Molecular Weight: | 140.91 g./mol | Molecular Formula: | C₅H₅BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03411559 | |
| Melting Point: | 177-178°C (dec.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic compounds, particularly in pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) targeting various diseases. Employed in the development of fluorinated pyridine derivatives, which are valuable in medicinal chemistry for their enhanced biological activity and metabolic stability. Also utilized in material science for creating advanced polymers and organic electronic materials. Its boronic acid group enables efficient conjugation with other molecules, making it a versatile building block in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 177 179? |
| Purity | 95.5 104.5% |
| APPEARANCE | WHITE TO ORANGE POWDER CRYSTALS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿480.00 |
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| 1.000 | 10-20 days | ฿820.00 |
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| 5.000 | 10-20 days | ฿1,430.00 |
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| 25.000 | 10-20 days | ฿5,382.00 |
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| 100.000 | 10-20 days | ฿19,080.00 |
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6-Fluoro-3-pyridinylboronic acid
Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex organic compounds, particularly in pharmaceuticals and agrochemicals. Acts as a key intermediate in the production of active pharmaceutical ingredients (APIs) targeting various diseases. Employed in the development of fluorinated pyridine derivatives, which are valuable in medicinal chemistry for their enhanced biological activity and metabolic stability. Also utilized in material science for creating advanced polymers and organic electronic materials. Its boronic acid group enables efficient conjugation with other molecules, making it a versatile building block in organic synthesis.
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