Methyl 4-(piperidin-3-yl)benzoate
95%
- Product Code: 83821
CAS:
927801-30-7
| Molecular Weight: | 219.28 g./mol | Molecular Formula: | C₁₃H₁₇NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09055085 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring both a piperidine ring and a benzoate ester, makes it a versatile building block for developing compounds with potential biological activity. It is often employed in the design and synthesis of molecules targeting central nervous system disorders, such as anxiety, depression, or neurodegenerative diseases, due to the piperidine moiety's ability to interact with neurotransmitter receptors. Additionally, the ester group allows for further chemical modifications, enabling the creation of prodrugs or enhancing the bioavailability of active pharmaceutical ingredients. Researchers also explore its use in the development of novel analgesics or anti-inflammatory agents, leveraging its structural features to optimize drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,098.00 |
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| 0.250 | 10-20 days | ฿16,821.00 |
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Methyl 4-(piperidin-3-yl)benzoate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring both a piperidine ring and a benzoate ester, makes it a versatile building block for developing compounds with potential biological activity. It is often employed in the design and synthesis of molecules targeting central nervous system disorders, such as anxiety, depression, or neurodegenerative diseases, due to the piperidine moiety's ability to interact with neurotransmitter receptors. Additionally, the ester group allows for further chemical modifications, enabling the creation of prodrugs or enhancing the bioavailability of active pharmaceutical ingredients. Researchers also explore its use in the development of novel analgesics or anti-inflammatory agents, leveraging its structural features to optimize drug efficacy and selectivity.
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