Pyrene-1-boronic acid
95.0%
- Product Code: 89514
CAS:
164461-18-1
| Molecular Weight: | 246.07 g./mol | Molecular Formula: | C₁₆H₁₁BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04974062 | |
| Melting Point: | 247-251 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8℃ |
Product Description:
Pyrene-1-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex aromatic compounds. It serves as a key building block in the development of organic electronic materials, such as OLEDs and organic semiconductors, due to its ability to form stable conjugated systems. Additionally, it is employed in the design of fluorescent probes and sensors for detecting biological molecules, leveraging its strong fluorescence properties. In materials science, it is utilized to modify surfaces and create functionalized polymers with specific optical or electronic characteristics. Its boronic acid group also makes it valuable in carbohydrate recognition and binding, aiding in biochemical research and diagnostics.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 95 105% |
| APPEARANCE | WHITE TO YELLOW TO BROWN POWDER AND/OR CHUNKS |
| INFRARED SPECTROMETRY | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $13.80 |
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| 5.000 | 10-20 days | $51.61 |
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| 25.000 | 10-20 days | $246.62 |
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Pyrene-1-boronic acid
Pyrene-1-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex aromatic compounds. It serves as a key building block in the development of organic electronic materials, such as OLEDs and organic semiconductors, due to its ability to form stable conjugated systems. Additionally, it is employed in the design of fluorescent probes and sensors for detecting biological molecules, leveraging its strong fluorescence properties. In materials science, it is utilized to modify surfaces and create functionalized polymers with specific optical or electronic characteristics. Its boronic acid group also makes it valuable in carbohydrate recognition and binding, aiding in biochemical research and diagnostics.
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