5-(2-Tolyl)thiazole-4-boronic acid pinacol ester
95%
- Product Code: 90770
CAS:
2223031-43-2
| Molecular Weight: | 319.22678 g./mol | Molecular Formula: | C₁₆H₂₂BNO₃S |
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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. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, agrochemicals, and advanced materials. Additionally, it is utilized in the synthesis of thiazole-containing compounds, which are often explored for their biological activities, such as antimicrobial and anticancer properties. 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 | ฿8,280.00 |
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| 0.025 | 10-20 days | ฿24,300.00 |
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5-(2-Tolyl)thiazole-4-boronic acid pinacol ester
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of drug candidates, agrochemicals, and advanced materials. Additionally, it is utilized in the synthesis of thiazole-containing compounds, which are often explored for their biological activities, such as antimicrobial and anticancer properties. Its stability and reactivity make it a preferred choice in medicinal chemistry and material science research.
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