2-Methoxy-3-pyridineboronic acid
97%
- Product Code: 89854
Alias:
2-Methoxypyridyl-3-boronic acid
CAS:
163105-90-6
| Molecular Weight: | 152.94 g./mol | Molecular Formula: | C₆H₈BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03411572 | |
| Melting Point: | 136-138°C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
2-Methoxy-3-pyridineboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various substrates. Its applications extend to research and industrial settings, where it aids in the discovery and optimization of new chemical entities.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 141 148? |
| PURITYHPLC | 97 100% |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $14.09 |
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| 5.000 | 10-20 days | $55.89 |
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| 25.000 | 10-20 days | $231.06 |
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| 100.000 | 10-20 days | $867.89 |
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2-Methoxy-3-pyridineboronic acid
2-Methoxy-3-pyridineboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various substrates. Its applications extend to research and industrial settings, where it aids in the discovery and optimization of new chemical entities.
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