(S)-1-(4-Fluorophenyl)ethanol

97%

  • Product Code: 113650
  CAS:    101219-73-2
Molecular Weight: 140.16 g./mol Molecular Formula: C₈H₉FO
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
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
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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