1-(4-Nitrophenyl)piperidin-4-yl methanesulfonate
≥95%
- Product Code: 39460
CAS:
303977-18-6
| Molecular Weight: | 300.33 g./mol | Molecular Formula: | C₁₂H₁₆N₂O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28405561 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
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. It is often employed in the development of compounds targeting the central nervous system, particularly in the design of potential antipsychotic or analgesic agents. The nitrophenyl and piperidinyl groups contribute to its ability to interact with specific biological receptors, making it valuable for drug discovery research. Additionally, its methanesulfonate moiety enhances its reactivity, facilitating further chemical modifications to create derivatives with optimized therapeutic properties. Researchers also explore its use in the study of enzyme inhibition and receptor binding mechanisms, aiding in the understanding of biochemical pathways and disease processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿4,644.00 |
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| 5.000 | 10-20 days | ฿9,288.00 |
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1-(4-Nitrophenyl)piperidin-4-yl methanesulfonate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. It is often employed in the development of compounds targeting the central nervous system, particularly in the design of potential antipsychotic or analgesic agents. The nitrophenyl and piperidinyl groups contribute to its ability to interact with specific biological receptors, making it valuable for drug discovery research. Additionally, its methanesulfonate moiety enhances its reactivity, facilitating further chemical modifications to create derivatives with optimized therapeutic properties. Researchers also explore its use in the study of enzyme inhibition and receptor binding mechanisms, aiding in the understanding of biochemical pathways and disease processes.
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