2-Methoxypyridne-4-boronic acid
95%
- Product Code: 89852
Alias:
2-methoxypyridine-4-boronic acid 2-methoxy-4-pyridine boronic acid 2-methoxy-4-pyridineboronic acid
CAS:
762262-09-9
| Molecular Weight: | 152.94 g./mol | Molecular Formula: | C₆H₈BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07368877 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
2-Methoxypyridine-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 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 biologically active compounds. Its boronic acid group enables efficient coupling with aryl or vinyl 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 organic and inorganic substrates. Its applications also extend to material science, where it contributes to the design of functional polymers and organic electronic materials.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 94.5 100% |
| APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿680.00 |
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| 1.000 | 10-20 days | ฿1,020.00 |
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| 5.000 | 10-20 days | ฿4,660.00 |
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| 25.000 | 10-20 days | ฿20,200.00 |
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2-Methoxypyridne-4-boronic acid
2-Methoxypyridine-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 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 biologically active compounds. Its boronic acid group enables efficient coupling with aryl or vinyl 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 organic and inorganic substrates. Its applications also extend to material science, where it contributes to the design of functional polymers and organic electronic materials.
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