3-Fluoro-5-(1H-pyrazol-1-yl)phenylboronic acid
95%
- Product Code: 91938
CAS:
2225169-96-8
| Molecular Weight: | 205.9814232 g./mol | Molecular Formula: | C₉H₈BFN₂O₂ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group allows it to form stable covalent bonds with various organic halides, facilitating the synthesis of biaryl compounds. These biaryl structures are often found in active pharmaceutical ingredients (APIs) and other biologically active molecules. Additionally, its pyrazole moiety enhances its versatility in designing compounds with specific biological activities, making it valuable in drug discovery and development. The fluorine atom in the structure can also influence the metabolic stability and binding affinity of the resulting molecules, further broadening its applications in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | Ft153,983.55 |
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| 0.025 | 10-20 days | Ft270,343.92 |
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3-Fluoro-5-(1H-pyrazol-1-yl)phenylboronic acid
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its boronic acid group allows it to form stable covalent bonds with various organic halides, facilitating the synthesis of biaryl compounds. These biaryl structures are often found in active pharmaceutical ingredients (APIs) and other biologically active molecules. Additionally, its pyrazole moiety enhances its versatility in designing compounds with specific biological activities, making it valuable in drug discovery and development. The fluorine atom in the structure can also influence the metabolic stability and binding affinity of the resulting molecules, further broadening its applications in medicinal chemistry.
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