(4-[(4-Fluorophenyl)Methyl]CarbamoylPhenyl)Boronic Acid
95%
- Product Code: 90458
CAS:
874460-12-5
| Molecular Weight: | 273.067 g./mol | Molecular Formula: | C₁₄H₁₃BFNO₃ |
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| EC Number: | MDL Number: | MFCD31648851 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for forming carbon-carbon bonds. Its boronic acid functional group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorine-substituted aromatic ring enhances its reactivity and selectivity in these reactions, making it suitable for constructing complex molecular structures. It is also explored in medicinal chemistry for designing drug candidates, particularly in targeting enzymes or receptors where the fluorine moiety can improve binding affinity and metabolic stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿4,572.00 |
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| 0.250 | 10-20 days | ฿18,180.00 |
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(4-[(4-Fluorophenyl)Methyl]CarbamoylPhenyl)Boronic Acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for forming carbon-carbon bonds. Its boronic acid functional group enables it to couple with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its fluorine-substituted aromatic ring enhances its reactivity and selectivity in these reactions, making it suitable for constructing complex molecular structures. It is also explored in medicinal chemistry for designing drug candidates, particularly in targeting enzymes or receptors where the fluorine moiety can improve binding affinity and metabolic stability.
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