Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate
95%
- Product Code: 39213
CAS:
318280-71-6
| Molecular Weight: | 233.7000 g./mol | Molecular Formula: | C₁₀H₁₆ClNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01480849 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring both a chloroacetyl group and a piperidine ring, makes it a versatile building block for designing compounds with potential therapeutic properties. It is often employed in the synthesis of analogs targeting neurological disorders, such as acetylcholinesterase inhibitors, which are used in the treatment of Alzheimer's disease. Additionally, it serves as a precursor in the development of compounds with potential anticancer, antimicrobial, or anti-inflammatory activities. Its reactivity allows for further functionalization, enabling researchers to explore diverse chemical modifications for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,440.00 |
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Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring both a chloroacetyl group and a piperidine ring, makes it a versatile building block for designing compounds with potential therapeutic properties. It is often employed in the synthesis of analogs targeting neurological disorders, such as acetylcholinesterase inhibitors, which are used in the treatment of Alzheimer's disease. Additionally, it serves as a precursor in the development of compounds with potential anticancer, antimicrobial, or anti-inflammatory activities. Its reactivity allows for further functionalization, enabling researchers to explore diverse chemical modifications for drug discovery and development.
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