4-(2-Fluorophenyl)thiazole-5-boronic acid pinacol ester
95%
- Product Code: 90339
CAS:
2223041-47-0
| Molecular Weight: | 323.1906632 g./mol | Molecular Formula: | C₁₅H₁₉BFNO₃S |
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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 building block for the introduction of the 4-(2-fluorophenyl)thiazole moiety into more complex molecules. Its boronic ester functional group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its stability and reactivity make it a preferred choice in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿10,080.00 |
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| 0.025 | 10-20 days | ฿29,304.00 |
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4-(2-Fluorophenyl)thiazole-5-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 building block for the introduction of the 4-(2-fluorophenyl)thiazole moiety into more complex molecules. Its boronic ester functional group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its stability and reactivity make it a preferred choice in medicinal chemistry and material science research.
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