3,5-Bis(imidazol-1-yl)phenylboronic acid
95%
- Product Code: 89922
CAS:
2225180-01-6
| Molecular Weight: | 254.05234 g./mol | Molecular Formula: | C₁₂H₁₁BN₄O₂ |
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| Density: | Storage Condition: | -20°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and materials science. It serves as a key building block in the development of supramolecular structures, particularly in the creation of coordination polymers and metal-organic frameworks (MOFs). Its boronic acid group enables it to participate in reversible covalent interactions, making it valuable for constructing dynamic and responsive materials. Additionally, it is employed in the design of sensors, especially for detecting sugars and other diol-containing molecules, due to its ability to form stable cyclic esters with these compounds. In medicinal chemistry, it is explored as a potential component in drug delivery systems, leveraging its binding affinity for biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $473.40 |
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| 0.025 | 10-20 days | $1,376.23 |
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3,5-Bis(imidazol-1-yl)phenylboronic acid
This compound is primarily utilized in the field of organic synthesis and materials science. It serves as a key building block in the development of supramolecular structures, particularly in the creation of coordination polymers and metal-organic frameworks (MOFs). Its boronic acid group enables it to participate in reversible covalent interactions, making it valuable for constructing dynamic and responsive materials. Additionally, it is employed in the design of sensors, especially for detecting sugars and other diol-containing molecules, due to its ability to form stable cyclic esters with these compounds. In medicinal chemistry, it is explored as a potential component in drug delivery systems, leveraging its binding affinity for biological targets.
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