5-(4-Fluorophenyl)thiazole-4-boronic acid pinacol ester
95%
- Product Code: 90800
CAS:
2223031-99-8
| 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 Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the attachment of aromatic or heteroaromatic systems. Its fluorophenyl moiety often contributes to the biological activity of the final compounds, making it valuable in drug discovery for targeting specific receptors or enzymes. Additionally, it is used in material science for the synthesis of organic electronic materials, where its structural properties can influence conductivity or optical characteristics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿8,280.00 |
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| 0.025 | 10-20 days | ฿24,300.00 |
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5-(4-Fluorophenyl)thiazole-4-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 the construction of complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the attachment of aromatic or heteroaromatic systems. Its fluorophenyl moiety often contributes to the biological activity of the final compounds, making it valuable in drug discovery for targeting specific receptors or enzymes. Additionally, it is used in material science for the synthesis of organic electronic materials, where its structural properties can influence conductivity or optical characteristics.
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