2-Cyclopentyl-6-(piperidin-3-yl)pyridine-4-boronic acid
95%
- Product Code: 59418
CAS:
2225152-32-7
| Molecular Weight: | 274.16632 g./mol | Molecular Formula: | C₁₅H₂₃BN₂O₂ |
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| Density: | Storage Condition: | -20℃, sealed and dry |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of novel drug candidates, particularly in the synthesis of small molecules targeting specific biological pathways. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the construction of complex organic molecules. Additionally, its structural features, including the cyclopentyl and piperidinyl groups, contribute to its potential in designing compounds with enhanced binding affinity and selectivity for biological targets, such as enzymes or receptors. This makes it a useful tool in medicinal chemistry for exploring new therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿86,080.00 |
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| 0.025 | 10-20 days | ฿223,800.00 |
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2-Cyclopentyl-6-(piperidin-3-yl)pyridine-4-boronic acid
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of novel drug candidates, particularly in the synthesis of small molecules targeting specific biological pathways. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the construction of complex organic molecules. Additionally, its structural features, including the cyclopentyl and piperidinyl groups, contribute to its potential in designing compounds with enhanced binding affinity and selectivity for biological targets, such as enzymes or receptors. This makes it a useful tool in medicinal chemistry for exploring new therapeutic agents.
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