3-Fluoro-5-(4-methylimidazol-1-yl)phenylboronic acid
95%
- Product Code: 91944
CAS:
2225155-55-3
| Molecular Weight: | 220.0080032 g./mol | Molecular Formula: | C₁₀H₁₀BFN₂O₂ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex molecules. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are essential in pharmaceuticals and agrochemicals. Additionally, the presence of the imidazole moiety enhances its utility in medicinal chemistry, as it can interact with biological targets, making it valuable in drug discovery for developing enzyme inhibitors or receptor modulators. Its fluorine substituent further contributes to its stability and bioavailability, making it a preferred choice in designing bioactive compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.010 | 10-20 days | $593.53 |
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| 0.025 | 10-20 days | $1,042.05 |
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3-Fluoro-5-(4-methylimidazol-1-yl)phenylboronic acid
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for constructing complex molecules. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are essential in pharmaceuticals and agrochemicals. Additionally, the presence of the imidazole moiety enhances its utility in medicinal chemistry, as it can interact with biological targets, making it valuable in drug discovery for developing enzyme inhibitors or receptor modulators. Its fluorine substituent further contributes to its stability and bioavailability, making it a preferred choice in designing bioactive compounds.
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