1-Benzylpiperidin-3-amine hydrochloride
95%
- Product Code: 117739
CAS:
368429-78-1
| Molecular Weight: | 226.75 g./mol | Molecular Formula: | C₁₂H₁₉ClN₂ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting the central nervous system, where it can be incorporated into molecules designed to interact with neurotransmitter receptors or enzymes. Additionally, it serves as a building block in the creation of potential therapeutic agents for conditions such as neurological disorders, pain management, and psychiatric illnesses. Its hydrochloride form enhances solubility, making it more suitable for use in experimental and formulation processes. Researchers also explore its derivatives for their potential in drug discovery and optimization, particularly in the design of ligands with improved binding affinity and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿864.00 |
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| 1.000 | 10-20 days | ฿2,088.00 |
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1-Benzylpiperidin-3-amine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting the central nervous system, where it can be incorporated into molecules designed to interact with neurotransmitter receptors or enzymes. Additionally, it serves as a building block in the creation of potential therapeutic agents for conditions such as neurological disorders, pain management, and psychiatric illnesses. Its hydrochloride form enhances solubility, making it more suitable for use in experimental and formulation processes. Researchers also explore its derivatives for their potential in drug discovery and optimization, particularly in the design of ligands with improved binding affinity and selectivity.
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