2-Fluoropyridine-4-boronic acid
95%
- Product Code: 67399
Alias:
2-Fluoro-4-pyridineboronic acid
CAS:
401815-98-3
| Molecular Weight: | 140.91 g./mol | Molecular Formula: | C₅H₅BFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04112534 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
2-Fluoropyridine-4-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making the compound valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group, enabling the coupling with various aryl or vinyl halides in the presence of a palladium catalyst. Additionally, the fluorine substituent on the pyridine ring can influence the electronic properties of the molecule, enhancing its reactivity or stability in specific applications. This compound is also utilized in the development of complex organic molecules, including bioactive compounds and ligands for catalysis. Its versatility makes it a crucial building block in medicinal chemistry and material science research.
Product Specification:
| Test | Specification |
|---|---|
| CARBON BY ELEMENTAL ANALYSIS | 41 42.9% |
| OXYGEN BY ELEMENTAL ANALYSIS | 21.5 23.2% |
| PURITYHPLC | 94.5 100% |
| INFRARED SPECTROMETRY | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
| APPEARANCE | White to off-white solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,280.00 |
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| 5.000 | 10-20 days | ฿4,420.00 |
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2-Fluoropyridine-4-boronic acid
2-Fluoropyridine-4-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making the compound valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group, enabling the coupling with various aryl or vinyl halides in the presence of a palladium catalyst. Additionally, the fluorine substituent on the pyridine ring can influence the electronic properties of the molecule, enhancing its reactivity or stability in specific applications. This compound is also utilized in the development of complex organic molecules, including bioactive compounds and ligands for catalysis. Its versatility makes it a crucial building block in medicinal chemistry and material science research.
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