(S)-2-amino-2-(3-fluoro-5-methoxyphenyl)ethanol hydrochloride
97%
- Product Code: 123711
CAS:
2095692-22-9
| Molecular Weight: | 221.66 g./mol | Molecular Formula: | C₉H₁₃ClFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24422017 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of drugs targeting neurological and psychiatric disorders, particularly those involving serotonin and dopamine pathways. Its structural features make it valuable for creating enantiomerically pure compounds, which are essential for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in research settings to study receptor binding activities and to develop novel treatments for conditions such as depression, anxiety, and Parkinson’s disease. Its fluorine and methoxy groups enhance its binding affinity and metabolic stability, making it a versatile building block in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿16,344.00 |
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(S)-2-amino-2-(3-fluoro-5-methoxyphenyl)ethanol hydrochloride
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a crucial role in the development of drugs targeting neurological and psychiatric disorders, particularly those involving serotonin and dopamine pathways. Its structural features make it valuable for creating enantiomerically pure compounds, which are essential for ensuring the efficacy and safety of therapeutic agents. Additionally, it is employed in research settings to study receptor binding activities and to develop novel treatments for conditions such as depression, anxiety, and Parkinson’s disease. Its fluorine and methoxy groups enhance its binding affinity and metabolic stability, making it a versatile building block in medicinal chemistry.
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