5-(3-Methylpiperidin-1-yl)furan-2-boronic acid pinacol ester
95%
- Product Code: 90783
CAS:
2223006-82-2
| Molecular Weight: | 309.20882 g./mol | Molecular Formula: | C₁₆H₂₈BNO₄ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic molecules, especially in the pharmaceutical industry. Its boronic ester functional group makes it valuable in Suzuki-Miyaura coupling reactions, which are widely employed to form carbon-carbon bonds. This enables the synthesis of various biologically active compounds, including potential drug candidates. Additionally, it may be used in the development of materials with specific electronic or optical properties, contributing to advancements in materials science. Its stability and reactivity make it a versatile tool in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $466.61 |
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| 0.100 | 10-20 days | $1,398.20 |
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5-(3-Methylpiperidin-1-yl)furan-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of complex organic molecules, especially in the pharmaceutical industry. Its boronic ester functional group makes it valuable in Suzuki-Miyaura coupling reactions, which are widely employed to form carbon-carbon bonds. This enables the synthesis of various biologically active compounds, including potential drug candidates. Additionally, it may be used in the development of materials with specific electronic or optical properties, contributing to advancements in materials science. Its stability and reactivity make it a versatile tool in modern synthetic chemistry.
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