4-(2-Methyl-4-fluorophenyl)thiazole-5-boronic acid pinacol ester
95%
- Product Code: 90344
CAS:
2223031-46-5
| Molecular Weight: | 337.2172432 g./mol | Molecular Formula: | C₁₆H₂₁BFNO₃S |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester functional group makes it a valuable building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the development of drug candidates, where it helps introduce the thiazole moiety into target molecules, enhancing their biological activity. Additionally, it is utilized in the synthesis of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to form stable carbon-carbon bonds under mild reaction conditions. Its fluorophenyl group further contributes to its utility in designing compounds with specific electronic and steric properties.
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-Methyl-4-fluorophenyl)thiazole-5-boronic acid pinacol ester
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic ester functional group makes it a valuable building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. It is often employed in the development of drug candidates, where it helps introduce the thiazole moiety into target molecules, enhancing their biological activity. Additionally, it is utilized in the synthesis of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to form stable carbon-carbon bonds under mild reaction conditions. Its fluorophenyl group further contributes to its utility in designing compounds with specific electronic and steric properties.
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