2-Methoxy-4-(2-methylimidazol-1-yl)phenylboronic acid
95%
- Product Code: 91708
CAS:
2225169-63-9
| Molecular Weight: | 232.04352 g./mol | Molecular Formula: | C₁₁H₁₃BN₂O₃ |
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| Density: | Storage Condition: | -20℃ |
Product Description:
This compound is primarily 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 materials science industries. Its boronic acid group allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, agrochemicals, and advanced materials. Additionally, its imidazole moiety can contribute to interactions with biological targets, making it useful in medicinal chemistry research for designing enzyme inhibitors or receptor modulators. Its applications also extend to the synthesis of fluorescent dyes and polymers, where its structural properties enhance functionality and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | Ft352,959.78 |
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2-Methoxy-4-(2-methylimidazol-1-yl)phenylboronic acid
This compound is primarily 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 materials science industries. Its boronic acid group allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the development of drugs, agrochemicals, and advanced materials. Additionally, its imidazole moiety can contribute to interactions with biological targets, making it useful in medicinal chemistry research for designing enzyme inhibitors or receptor modulators. Its applications also extend to the synthesis of fluorescent dyes and polymers, where its structural properties enhance functionality and stability.
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