(R)-2-Chloro-1-(4-fluorophenyl)ethanol
≥98%
- Product Code: 84839
CAS:
126534-43-8
| Molecular Weight: | 174.60 g./mol | Molecular Formula: | C₈H₈ClFO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08064295 | |
| Melting Point: | Boiling Point: | 256.6 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the production of chiral molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable building block for creating active pharmaceutical ingredients (APIs) with specific stereochemistry. It is often employed in the development of drugs targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. The compound is also used in research settings to study the effects of stereochemistry on biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,125.00 |
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| 1.000 | 10-20 days | ฿2,799.00 |
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| 5.000 | 10-20 days | ฿10,080.00 |
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(R)-2-Chloro-1-(4-fluorophenyl)ethanol
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the production of chiral molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable building block for creating active pharmaceutical ingredients (APIs) with specific stereochemistry. It is often employed in the development of drugs targeting central nervous system disorders, cardiovascular diseases, and other therapeutic areas. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. The compound is also used in research settings to study the effects of stereochemistry on biological activity.
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