4-(2-Methylpiperidin-1-yl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90348
CAS:
2223009-25-2
| Molecular Weight: | 325.27442 g./mol | Molecular Formula: | C₁₆H₂₈BNO₃S |
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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 such as Suzuki-Miyaura coupling. It serves as a crucial intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it finds use in materials science for synthesizing organic electronic materials, including polymers and small molecules for optoelectronic applications. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿15,552.00 |
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| 0.100 | 10-20 days | ฿46,602.00 |
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4-(2-Methylpiperidin-1-yl)thiophene-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a crucial intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of active pharmaceutical ingredients (APIs) and other fine chemicals. Additionally, it finds use in materials science for synthesizing organic electronic materials, including polymers and small molecules for optoelectronic applications. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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