(3-(Phenylcarbamoyl)phenyl)boronic acid
98%
- Product Code: 90286
CAS:
397843-71-9
| Molecular Weight: | 241.05 g./mol | Molecular Formula: | C₁₃H₁₂BNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04115711 | |
| Melting Point: | 250-260°C | Boiling Point: | |
| Density: | 1.28g/mL | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceuticals and materials science. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds in drug discovery and development. Additionally, it finds application in the preparation of bioactive compounds and organic electronic materials due to its ability to introduce phenylcarbamoyl groups into target molecules. Its role in catalysis and functional material synthesis further highlights its versatility in advanced chemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,650.00 |
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| 1.000 | 10-20 days | ฿7,860.00 |
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(3-(Phenylcarbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceuticals and materials science. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds in drug discovery and development. Additionally, it finds application in the preparation of bioactive compounds and organic electronic materials due to its ability to introduce phenylcarbamoyl groups into target molecules. Its role in catalysis and functional material synthesis further highlights its versatility in advanced chemical research.
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