5-(Diethylamino)thiophene-2-boronic acid pinacol ester
95%
- Product Code: 90827
CAS:
2223046-09-9
| Molecular Weight: | 299.23714 g./mol | Molecular Formula: | C₁₄H₂₆BNO₃S |
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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 building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it is used in materials science for the development of organic electronic materials, such as conductive polymers and organic light-emitting diodes (OLEDs), due to the electron-rich nature of the thiophene ring.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $466.61 |
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| 0.100 | 10-20 days | $1,398.20 |
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5-(Diethylamino)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 building block for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of diverse thiophene derivatives. These derivatives are often explored for their potential biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, it is used in materials science for the development of organic electronic materials, such as conductive polymers and organic light-emitting diodes (OLEDs), due to the electron-rich nature of the thiophene ring.
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