(3-(Diethylcarbamoyl)phenyl)boronic acid
97%
- Product Code: 44440
CAS:
237413-05-7
Molecular Weight: | 221.0600 g./mol | Molecular Formula: | C₁₁H₁₆BNO₃ |
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EC Number: | MDL Number: | MFCD04115684 | |
Melting Point: | Boiling Point: | 436.4 °C at 760 mmHg | |
Density: | 1.14g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid moiety allows for selective and efficient coupling with aryl halides or triflates in the presence of a palladium catalyst. Additionally, it finds application in the development of sensors and probes due to its ability to interact with diols and other biomolecules, making it valuable in biochemical research and diagnostics.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,098.00 |
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(3-(Diethylcarbamoyl)phenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid moiety allows for selective and efficient coupling with aryl halides or triflates in the presence of a palladium catalyst. Additionally, it finds application in the development of sensors and probes due to its ability to interact with diols and other biomolecules, making it valuable in biochemical research and diagnostics.
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