Pinacol 4-(3,4-dimethoxypyridine-2-ylmethoxy) phenylboronic acid pinacol ester
95%
- Product Code: 46182
CAS:
1300645-77-5
| Molecular Weight: | 371.23514 g./mol | Molecular Formula: | C₂₀H₂₆BNO₅ |
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| Density: | Storage Condition: | 2-8℃ |
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 boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. Its structure, featuring a dimethoxypyridine moiety, enhances stability and reactivity, making it suitable for constructing complex organic molecules. Applications include the synthesis of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the development of bioactive compounds and ligands for catalysis, leveraging its ability to facilitate selective and efficient coupling processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿16,880.00 |
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| 1.000 | 10-20 days | ฿42,880.00 |
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| 5.000 | 10-20 days | ฿108,800.00 |
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Pinacol 4-(3,4-dimethoxypyridine-2-ylmethoxy) phenylboronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. Its structure, featuring a dimethoxypyridine moiety, enhances stability and reactivity, making it suitable for constructing complex organic molecules. Applications include the synthesis of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the development of bioactive compounds and ligands for catalysis, leveraging its ability to facilitate selective and efficient coupling processes.
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