(4-Carbamoyl-2-fluorophenyl)boronic acid
98%
- Product Code: 90617
CAS:
874289-22-2
| Molecular Weight: | 182.94 g./mol | Molecular Formula: | C₇H₇BFNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09800867 | |
| Melting Point: | Boiling Point: | 359.8°C | |
| Density: | 1.41g/mL | Storage Condition: | 2-8°C |
Product Description:
(4-Carbamoyl-2-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the formation of complex organic molecules. Additionally, it is utilized in the development of bioactive compounds and drug candidates due to its ability to interact with biological targets. Its fluorophenyl moiety further enhances its utility in creating compounds with specific electronic and steric properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,380.00 |
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| 1.000 | 10-20 days | ฿10,000.00 |
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(4-Carbamoyl-2-fluorophenyl)boronic acid
(4-Carbamoyl-2-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the formation of complex organic molecules. Additionally, it is utilized in the development of bioactive compounds and drug candidates due to its ability to interact with biological targets. Its fluorophenyl moiety further enhances its utility in creating compounds with specific electronic and steric properties.
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