4-(4-Methoxyphenyl)thiazole-5-boronic acid pinacol ester
95%
- Product Code: 90432
CAS:
2223053-39-0
| Molecular Weight: | 335.22618 g./mol | Molecular Formula: | C₁₆H₂₂BNO₄S |
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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 functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, it is employed in material science for the creation of organic electronic materials, where its structural properties contribute to the development of advanced polymers or small-molecule semiconductors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.005 | 10-20 days | $396.41 |
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| 0.025 | 10-20 days | $1,152.41 |
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4-(4-Methoxyphenyl)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 functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Additionally, it is employed in material science for the creation of organic electronic materials, where its structural properties contribute to the development of advanced polymers or small-molecule semiconductors.
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