N-Ethyl-1-(pyridin-4-yl)piperidin-4-amine
95%
- Product Code: 124547
CAS:
1094514-08-5
| Molecular Weight: | 205.30 g./mol | Molecular Formula: | C₁₂H₁₉N₃ |
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| EC Number: | MDL Number: | MFCD3920912 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry, protected from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting the central nervous system. Its structural features make it suitable for designing molecules that interact with specific receptors or enzymes in the brain, potentially leading to treatments for neurological disorders such as depression, anxiety, or schizophrenia. Additionally, it may be explored for its potential in developing compounds with analgesic or anti-inflammatory properties. Researchers also investigate its role in the creation of novel bioactive molecules for other therapeutic areas, leveraging its piperidine and pyridine moieties for enhanced binding affinity and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $319.12 |
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| 0.250 | 10-20 days | $478.47 |
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| 1.000 | 10-20 days | $1,195.33 |
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N-Ethyl-1-(pyridin-4-yl)piperidin-4-amine
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting the central nervous system. Its structural features make it suitable for designing molecules that interact with specific receptors or enzymes in the brain, potentially leading to treatments for neurological disorders such as depression, anxiety, or schizophrenia. Additionally, it may be explored for its potential in developing compounds with analgesic or anti-inflammatory properties. Researchers also investigate its role in the creation of novel bioactive molecules for other therapeutic areas, leveraging its piperidine and pyridine moieties for enhanced binding affinity and selectivity.
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