4-(2-Trifluoromethylphenyl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90355
CAS:
2223042-41-7
| Molecular Weight: | 372.2101096 g./mol | Molecular Formula: | C₁₇H₂₀BF₃O₃S |
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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 thiophene derivatives into more complex molecules, which are often used in the development of pharmaceuticals and organic electronic materials. Its trifluoromethylphenyl group enhances the stability and reactivity of the compound, making it valuable in the creation of advanced materials with specific electronic properties. Additionally, it is employed in the synthesis of compounds for research in medicinal chemistry, where the thiophene moiety can contribute to the biological activity of the final product.
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 | ฿46,674.00 |
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4-(2-Trifluoromethylphenyl)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 building block for the introduction of thiophene derivatives into more complex molecules, which are often used in the development of pharmaceuticals and organic electronic materials. Its trifluoromethylphenyl group enhances the stability and reactivity of the compound, making it valuable in the creation of advanced materials with specific electronic properties. Additionally, it is employed in the synthesis of compounds for research in medicinal chemistry, where the thiophene moiety can contribute to the biological activity of the final product.
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