4-(Imidazol-1-yl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90493
CAS:
2223032-27-5
| 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 Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of thiophene-based materials, which are essential in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its imidazole moiety further enhances its utility in designing biologically active compounds, including potential drug candidates targeting various diseases.
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-(Imidazol-1-yl)thiophene-2-boronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of thiophene-based materials, which are essential in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its imidazole moiety further enhances its utility in designing biologically active compounds, including potential drug candidates targeting various diseases.
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