4-(2-Trifluoromethylphenyl)thiazole-5-boronic acid pinacol ester
95%
- Product Code: 90354
CAS:
2223039-30-1
| Molecular Weight: | 373.1981696 g./mol | Molecular Formula: | C₁₆H₁₉BF₃NO₃S |
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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 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 the synthesis of biologically active compounds, including potential drug candidates. Additionally, its trifluoromethylphenyl group can enhance the metabolic stability and lipophilicity of the resulting molecules, which is beneficial in drug design.
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-Trifluoromethylphenyl)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 intermediate for constructing complex 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 the synthesis of biologically active compounds, including potential drug candidates. Additionally, its trifluoromethylphenyl group can enhance the metabolic stability and lipophilicity of the resulting molecules, which is beneficial in drug design.
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