3-Cyclohexylthiophene-2-boronic acid pinacol ester
95%
- Product Code: 90061
CAS:
2223051-24-7
| Molecular Weight: | 310.25978 g./mol | Molecular Formula: | C₁₆H₂₇BO₃S |
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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 key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in creating biologically active compounds or functional materials. Additionally, it finds applications in material science, particularly in the synthesis of conjugated polymers or organic electronic materials, where its thiophene moiety contributes to electronic properties. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿11,682.00 |
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| 0.025 | 10-20 days | ฿34,254.00 |
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3-Cyclohexylthiophene-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 key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in creating biologically active compounds or functional materials. Additionally, it finds applications in material science, particularly in the synthesis of conjugated polymers or organic electronic materials, where its thiophene moiety contributes to electronic properties. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.
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