5-(4-Tolyl)thiazole-4-boronic acid pinacol ester
95%
- Product Code: 90813
CAS:
2223044-52-6
| 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 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 bioactive compounds, including potential drug candidates. Additionally, it is employed in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity under mild conditions make it a versatile tool in modern synthetic chemistry.
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-Tolyl)thiazole-4-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 bioactive compounds, including potential drug candidates. Additionally, it is employed in material science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity under mild conditions make it a versatile tool in modern synthetic chemistry.
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