5-(1H-Pyrazol-1-yl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90757
CAS:
2223032-96-8
| Molecular Weight: | 294.17756 g./mol | Molecular Formula: | C₁₃H₁₉BN₂O₃S |
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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 the Suzuki-Miyaura reaction. It serves as a key 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, its pyrazole moiety contributes to its use in designing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a versatile reagent in medicinal chemistry and material science research.
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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5-(1H-Pyrazol-1-yl)thiophene-2-boronic 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 key 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, its pyrazole moiety contributes to its use in designing compounds with potential biological activity, such as enzyme inhibitors or receptor modulators. Its stability and reactivity make it a versatile reagent in medicinal chemistry and material science research.
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