5-(1-Methyl-1-acetoxyethyl)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90755
CAS:
1402174-74-6
| Molecular Weight: | 328.232 g./mol | Molecular Formula: | C₁₅H₂₅BO₅S |
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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 organic 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. Additionally, it finds application in material science for the synthesis of conjugated polymers and organic electronic materials, where thiophene derivatives are often employed due to their desirable electronic properties. The compound’s stability and reactivity make it a valuable tool in research and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | Ft482,680.04 |
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| 0.100 | 10-20 days | Ft1,448,040.12 |
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5-(1-Methyl-1-acetoxyethyl)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 intermediate for constructing complex organic 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. Additionally, it finds application in material science for the synthesis of conjugated polymers and organic electronic materials, where thiophene derivatives are often employed due to their desirable electronic properties. The compound’s stability and reactivity make it a valuable tool in research and industrial processes.
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