Pinacol 4-((pyridine-2-yl) methoxy) phenylboronic acid pinacol ester
95%
- Product Code: 46054
CAS:
1276129-55-5
| Molecular Weight: | 311.18318 g./mol | Molecular Formula: | C₁₈H₂₂BNO₃ |
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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 acid ester reagent, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its structure, featuring a pyridine moiety, enhances its stability and reactivity in various catalytic processes. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. Additionally, its boronic ester group allows for selective transformations in medicinal chemistry, aiding in the development of drug candidates and bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,872.00 |
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| 0.250 | 10-20 days | ฿3,339.00 |
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| 1.000 | 10-20 days | ฿9,000.00 |
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Pinacol 4-((pyridine-2-yl) methoxy) 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 acid ester reagent, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its structure, featuring a pyridine moiety, enhances its stability and reactivity in various catalytic processes. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. Additionally, its boronic ester group allows for selective transformations in medicinal chemistry, aiding in the development of drug candidates and bioactive compounds.
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