(R)-6-Methoxychroman-4-amine
95%
- Product Code: 37726
CAS:
1018978-89-6
| Molecular Weight: | 179.22 g./mol | Molecular Formula: | C₁₀H₁₃NO₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
(R)-6-Methoxychroman-4-amine is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting the central nervous system. The compound is often employed in the production of serotonin receptor agonists and antagonists, which are crucial for treating psychiatric and neurological disorders such as depression, anxiety, and migraines. Additionally, it serves as a building block in the synthesis of compounds with potential antioxidant and neuroprotective properties, making it relevant in research focused on neurodegenerative diseases like Alzheimer's and Parkinson's. Its methoxy and amine functional groups also allow for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿17,856.00 |
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(R)-6-Methoxychroman-4-amine
(R)-6-Methoxychroman-4-amine is primarily used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, particularly those targeting the central nervous system. The compound is often employed in the production of serotonin receptor agonists and antagonists, which are crucial for treating psychiatric and neurological disorders such as depression, anxiety, and migraines. Additionally, it serves as a building block in the synthesis of compounds with potential antioxidant and neuroprotective properties, making it relevant in research focused on neurodegenerative diseases like Alzheimer's and Parkinson's. Its methoxy and amine functional groups also allow for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and development.
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