(1-Isopropylpiperidin-4-yl)methanol
95%
- Product Code: 36133
CAS:
280774-03-0
| Molecular Weight: | 157.2533 g./mol | Molecular Formula: | C₉H₁₉NO |
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| EC Number: | MDL Number: | MFCD08059811 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
(1-Isopropylpiperidin-4-yl)methanol is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting the central nervous system. The compound's structure, featuring a piperidine ring and an isopropyl group, makes it a valuable building block for developing drugs with potential applications in treating neurological disorders, such as Parkinson's disease, Alzheimer's disease, and other conditions involving dopamine regulation. Additionally, it is explored in the development of antipsychotic and analgesic agents due to its ability to interact with neurotransmitter receptors. Its versatility in organic synthesis also extends to the creation of novel compounds for pharmacological screening and drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,898.00 |
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(1-Isopropylpiperidin-4-yl)methanol
(1-Isopropylpiperidin-4-yl)methanol is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting the central nervous system. The compound's structure, featuring a piperidine ring and an isopropyl group, makes it a valuable building block for developing drugs with potential applications in treating neurological disorders, such as Parkinson's disease, Alzheimer's disease, and other conditions involving dopamine regulation. Additionally, it is explored in the development of antipsychotic and analgesic agents due to its ability to interact with neurotransmitter receptors. Its versatility in organic synthesis also extends to the creation of novel compounds for pharmacological screening and drug discovery programs.
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