4-[4-(2-Chloroethyl)-1-piperidinyl] benzoic acid methyl ester
95%
- Product Code: 84692
CAS:
936130-71-1
| Molecular Weight: | 281.7778 g./mol | Molecular Formula: | C₁₅H₂₀ClNO₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 420.3±20.0 °C | |
| Density: | 1.133±0.06 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various pharmacologically active compounds, particularly those targeting neurological and cardiovascular systems. Its structure, featuring a piperidine ring and a chloroethyl group, makes it valuable for developing molecules with potential receptor-binding properties. Researchers often employ it to create analogs for studying drug-receptor interactions or to modify existing drugs to enhance their efficacy or reduce side effects. Additionally, it may be used in the development of prodrugs, where its ester group can be hydrolyzed in vivo to release the active therapeutic agent. Its applications are largely confined to laboratory settings, focusing on drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿9,072.00 |
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| 0.250 | 10-20 days | ฿32,688.00 |
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4-[4-(2-Chloroethyl)-1-piperidinyl] benzoic acid methyl ester
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various pharmacologically active compounds, particularly those targeting neurological and cardiovascular systems. Its structure, featuring a piperidine ring and a chloroethyl group, makes it valuable for developing molecules with potential receptor-binding properties. Researchers often employ it to create analogs for studying drug-receptor interactions or to modify existing drugs to enhance their efficacy or reduce side effects. Additionally, it may be used in the development of prodrugs, where its ester group can be hydrolyzed in vivo to release the active therapeutic agent. Its applications are largely confined to laboratory settings, focusing on drug discovery and development processes.
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