4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-carbaldehyde
97%
- Product Code: 242611
CAS:
846023-58-3
| Molecular Weight: | 222.05 g./mol | Molecular Formula: | C₁₁H₁₅BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06657890 | |
| Melting Point: | Boiling Point: | 338.1 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, inert gas storage |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic systems. Its aldehyde and boronate functional groups allow for sequential or selective transformations, making it valuable in the preparation of complex molecules such as pharmaceuticals, agrochemicals, and conjugated materials for optoelectronics. The compound serves as a versatile building block in medicinal chemistry due to its ability to introduce furan rings into larger frameworks, which are often associated with bioactive properties. It is also employed in the synthesis of fluorescent dyes and organic semiconductors owing to the electron-rich nature of the furan moiety.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | €34.26 |
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| 5g | 10-20 days | €171.29 |
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| 25g | 10-20 days | €747.90 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)furan-2-carbaldehyde
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds between aromatic systems. Its aldehyde and boronate functional groups allow for sequential or selective transformations, making it valuable in the preparation of complex molecules such as pharmaceuticals, agrochemicals, and conjugated materials for optoelectronics. The compound serves as a versatile building block in medicinal chemistry due to its ability to introduce furan rings into larger frameworks, which are often associated with bioactive properties. It is also employed in the synthesis of fluorescent dyes and organic semiconductors owing to the electron-rich nature of the furan moiety.
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