Chroman-6-amine hydrochloride
95%
- Product Code: 52518
CAS:
2250243-12-8
| Molecular Weight: | 185.6507 g./mol | Molecular Formula: | C₉H₁₂ClNO |
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| EC Number: | MDL Number: | MFCD28894937 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting neurological disorders, such as depression and anxiety, due to its amine functional group and chroman backbone, which are often found in bioactive molecules. Additionally, it serves as a building block in the creation of potential therapeutic agents for cardiovascular diseases, where its structural framework can be modified to enhance activity and selectivity. Researchers also explore its use in designing novel antioxidants, leveraging the chroman moiety's inherent ability to scavenge free radicals. Its hydrochloride form ensures stability and solubility, making it suitable for laboratory-scale synthesis and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft162,807.55 |
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Chroman-6-amine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting neurological disorders, such as depression and anxiety, due to its amine functional group and chroman backbone, which are often found in bioactive molecules. Additionally, it serves as a building block in the creation of potential therapeutic agents for cardiovascular diseases, where its structural framework can be modified to enhance activity and selectivity. Researchers also explore its use in designing novel antioxidants, leveraging the chroman moiety's inherent ability to scavenge free radicals. Its hydrochloride form ensures stability and solubility, making it suitable for laboratory-scale synthesis and drug discovery processes.
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