(S)-1-(4-Fluorophenyl)ethanol
97%
- Product Code: 113650
CAS:
101219-73-2
Molecular Weight: | 140.16 g./mol | Molecular Formula: | C₈H₉FO |
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EC Number: | MDL Number: | MFCD03092998 | |
Melting Point: | Boiling Point: | 216.2°C at 760 mmHg | |
Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
(S)-1-(4-Fluorophenyl)ethanol is widely used as an intermediate in the synthesis of various pharmaceuticals, particularly in the production of chiral drugs. Its enantiomeric purity makes it valuable for creating active pharmaceutical ingredients (APIs) with specific stereochemical requirements. This compound is often employed in the development of antidepressants, antipsychotics, and other central nervous system (CNS) drugs due to its structural compatibility with bioactive molecules. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules through reactions like esterification, etherification, or further functional group transformations. Its role in asymmetric synthesis also contributes to the production of high-purity compounds for research and industrial applications.
Product Specification:
Test | Specification |
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Appearance | Colourless To Yellow Liquid |
Purity (%) | 96.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Specific Rotation [a]20/D (C=1 In Chloroform) | -45-53 |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $58.20 |
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0.250 | 10-20 days | $85.34 |
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1.000 | 10-20 days | $233.99 |
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(S)-1-(4-Fluorophenyl)ethanol
(S)-1-(4-Fluorophenyl)ethanol is widely used as an intermediate in the synthesis of various pharmaceuticals, particularly in the production of chiral drugs. Its enantiomeric purity makes it valuable for creating active pharmaceutical ingredients (APIs) with specific stereochemical requirements. This compound is often employed in the development of antidepressants, antipsychotics, and other central nervous system (CNS) drugs due to its structural compatibility with bioactive molecules. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules through reactions like esterification, etherification, or further functional group transformations. Its role in asymmetric synthesis also contributes to the production of high-purity compounds for research and industrial applications.
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