(4-(Diethylcarbamoyl)-3-fluorophenyl)boronic acid
98%
- Product Code: 90528
CAS:
874289-14-2
| Molecular Weight: | 239.05 g./mol | Molecular Formula: | C₁₁H₁₅BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08436057 | |
| Melting Point: | 158-160°C | Boiling Point: | 433.3°C |
| Density: | 1.21g/mL | Storage Condition: | 2-8°C |
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. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, the presence of the diethylcarbamoyl and fluorine groups can enhance its reactivity and selectivity in specific reactions, contributing to the development of novel compounds with potential applications in drug discovery and advanced materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,360.00 |
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| 1.000 | 10-20 days | ฿6,360.00 |
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| 5.000 | 10-20 days | ฿22,230.00 |
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(4-(Diethylcarbamoyl)-3-fluorophenyl)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. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, the presence of the diethylcarbamoyl and fluorine groups can enhance its reactivity and selectivity in specific reactions, contributing to the development of novel compounds with potential applications in drug discovery and advanced materials.
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