(S)-1-(3-Fluoro-4-nitrophenyl)ethanol
95%
- Product Code: 233319
CAS:
2097713-63-6
| Molecular Weight: | 185.15 g./mol | Molecular Formula: | C₈H₈FNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31417450 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, light-proof, inert gas |
Product Description:
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure contains both a fluorine atom and a nitro group, making it a valuable building block for further functionalization through reduction or nucleophilic substitution reactions. Commonly employed in the preparation of fluorinated bioactive molecules, including potential candidates in anti-inflammatory, antimicrobial, or central nervous system agents. The presence of the chiral center allows for selective interactions in biological systems, enhancing drug efficacy and reducing side effects when used in enantiomerically pure form.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $844.62 |
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| 0.250 | 10-20 days | $1,436.06 |
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(S)-1-(3-Fluoro-4-nitrophenyl)ethanol
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure contains both a fluorine atom and a nitro group, making it a valuable building block for further functionalization through reduction or nucleophilic substitution reactions. Commonly employed in the preparation of fluorinated bioactive molecules, including potential candidates in anti-inflammatory, antimicrobial, or central nervous system agents. The presence of the chiral center allows for selective interactions in biological systems, enhancing drug efficacy and reducing side effects when used in enantiomerically pure form.
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