(R)-2-(1-Amino-2-hydroxyethyl)-5-fluorophenol hydrochloride
95%
- Product Code: 123670
CAS:
2177257-85-9
| Molecular Weight: | 207.62 g./mol | Molecular Formula: | C₈H₁₁ClFNO₂ |
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| EC Number: | MDL Number: | MFCD24434070 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring both amino and hydroxyl groups, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs) targeting neurological and cardiovascular disorders. The fluorine atom enhances its binding affinity to specific biological targets, making it useful in the design of receptor-specific drugs. Additionally, it is employed in the study of enzyme inhibition and as a building block for complex organic molecules in medicinal chemistry. Its chiral nature is particularly important in the development of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,240.00 |
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| 0.250 | 10-20 days | ฿18,324.00 |
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| 1.000 | 10-20 days | ฿45,792.00 |
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(R)-2-(1-Amino-2-hydroxyethyl)-5-fluorophenol hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of chiral molecules. Its structure, featuring both amino and hydroxyl groups, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs) targeting neurological and cardiovascular disorders. The fluorine atom enhances its binding affinity to specific biological targets, making it useful in the design of receptor-specific drugs. Additionally, it is employed in the study of enzyme inhibition and as a building block for complex organic molecules in medicinal chemistry. Its chiral nature is particularly important in the development of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects.
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