4-hydroxy-2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
97%(HPLC)
- Product Code: 46699
CAS:
1883607-86-0
| Molecular Weight: | 248.08 g./mol | Molecular Formula: | C₁₃H₁₇BO₄ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic structures. Additionally, it serves as a precursor in the development of fluorescent probes and sensors, leveraging its aldehyde functionality for further derivatization. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing drug candidates and bioactive molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £203.55 |
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4-hydroxy-2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various boron-containing molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group in the compound facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic structures. Additionally, it serves as a precursor in the development of fluorescent probes and sensors, leveraging its aldehyde functionality for further derivatization. Its stability and reactivity make it a versatile tool in medicinal chemistry for designing drug candidates and bioactive molecules.
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