(S)-1-(4-(Trifluoromethoxy)phenyl)propan-1-amine hydrochloride
95%
- Product Code: 37910
CAS:
1391484-89-1
| Molecular Weight: | 255.6645 g./mol | Molecular Formula: | C₁₀H₁₃ClF₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12757228 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting the central nervous system. Its structure, featuring a trifluoromethoxy group, enhances its potential in developing compounds with improved metabolic stability and binding affinity. Researchers often employ it in the design of drugs for neurological disorders, such as depression, anxiety, and other mood-related conditions. Additionally, its chiral nature allows for the exploration of enantioselective interactions in drug development, contributing to the creation of more effective and targeted therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,976.00 |
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(S)-1-(4-(Trifluoromethoxy)phenyl)propan-1-amine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting the central nervous system. Its structure, featuring a trifluoromethoxy group, enhances its potential in developing compounds with improved metabolic stability and binding affinity. Researchers often employ it in the design of drugs for neurological disorders, such as depression, anxiety, and other mood-related conditions. Additionally, its chiral nature allows for the exploration of enantioselective interactions in drug development, contributing to the creation of more effective and targeted therapies.
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