4-(2-Thienyl)piperidine
≥98%
- Product Code: 118514
CAS:
198334-38-2
| Molecular Weight: | 167.27 g./mol | Molecular Formula: | C₉H₁₃NS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12027113 | |
| Melting Point: | 46-50°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a building block for the synthesis of various pharmacologically active molecules. Its structure, featuring a piperidine ring linked to a thienyl group, makes it a valuable intermediate in the development of compounds targeting the central nervous system. It has been explored in the creation of potential therapeutic agents for neurological disorders, including antidepressants, antipsychotics, and analgesics. Additionally, its unique chemical framework is studied for its potential in designing ligands for receptor modulation, particularly in the development of drugs that interact with dopamine or serotonin receptors. Its applications also extend to research in organic synthesis, where it serves as a precursor for more complex heterocyclic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €336.63 |
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4-(2-Thienyl)piperidine
This compound is primarily utilized in the field of medicinal chemistry as a building block for the synthesis of various pharmacologically active molecules. Its structure, featuring a piperidine ring linked to a thienyl group, makes it a valuable intermediate in the development of compounds targeting the central nervous system. It has been explored in the creation of potential therapeutic agents for neurological disorders, including antidepressants, antipsychotics, and analgesics. Additionally, its unique chemical framework is studied for its potential in designing ligands for receptor modulation, particularly in the development of drugs that interact with dopamine or serotonin receptors. Its applications also extend to research in organic synthesis, where it serves as a precursor for more complex heterocyclic compounds.
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