(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid
95%
- Product Code: 113362
CAS:
1000269-51-1
| Molecular Weight: | 257.05 g./mol | Molecular Formula: | C₁₃H₁₂BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16038213 | |
| Melting Point: | Boiling Point: | 495.051 °C at 760 mmHg | |
| Density: | 1.312 g/cm3 | Storage Condition: | 2-8°C, inert gas |
Product Description:
(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules, including potential drug candidates. The boronic acid group in the compound facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in many bioactive compounds. Additionally, it can be used in the development of materials science, particularly in the synthesis of organic electronic materials. Its role in these applications highlights its importance in advancing both medicinal chemistry and material innovation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,971.00 |
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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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(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid
(6-((Benzyloxy)carbonyl)pyridin-3-yl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry to create complex molecules, including potential drug candidates. The boronic acid group in the compound facilitates the formation of carbon-carbon bonds, making it valuable for constructing biaryl structures, which are common in many bioactive compounds. Additionally, it can be used in the development of materials science, particularly in the synthesis of organic electronic materials. Its role in these applications highlights its importance in advancing both medicinal chemistry and material innovation.
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