4-(6-Cyanopyridin-2-ylcarbamoyl)phenylboronic acid
95%
- Product Code: 46373
CAS:
2243290-83-5
| Molecular Weight: | 267.05 g./mol | Molecular Formula: | C₁₃H₁₀BN₃O₃ |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its unique structure, which combines boronic acid and pyridine moieties. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of kinase inhibitors, which are important for treating various cancers and inflammatory diseases. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Additionally, its pyridine component enhances its ability to interact with biological targets, making it valuable in the design of bioactive molecules. The compound is also explored in the development of sensors and probes for detecting specific analytes due to its selective binding properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | €1,132.58 |
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4-(6-Cyanopyridin-2-ylcarbamoyl)phenylboronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its unique structure, which combines boronic acid and pyridine moieties. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of kinase inhibitors, which are important for treating various cancers and inflammatory diseases. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Additionally, its pyridine component enhances its ability to interact with biological targets, making it valuable in the design of bioactive molecules. The compound is also explored in the development of sensors and probes for detecting specific analytes due to its selective binding properties.
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