(R)-1-(4-Fluorophenyl)ethanol

97%

  • Product Code: 84834
  CAS:    101219-68-5
Molecular Weight: 140.16 g./mol Molecular Formula: C₈H₉FO
EC Number: MDL Number: MFCD03092997
Melting Point: Boiling Point: 9092°C at 7 mmHg
Density: Storage Condition: Room temperature, dry and sealed
Product Description: This chemical is primarily used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds. Its chiral nature makes it valuable for creating enantiomerically pure drugs, which are essential for ensuring specific biological activity and reducing side effects. It is often employed in the development of antidepressants, antipsychotics, and other central nervous system (CNS) drugs. Additionally, it serves as a building block in organic synthesis for creating complex molecules with potential therapeutic applications. Its fluorine atom enhances the stability and bioavailability of the resulting compounds, making it a key component in medicinal chemistry research.
Product Specification:
Test Specification
APPEARANCE colourless liquid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Specific rotation a20D C1 in Chloroform 45-53
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿470.00
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-
0.250 10-20 days ฿680.00
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1.000 10-20 days ฿2,160.00
+
-
5.000 10-20 days ฿8,780.00
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(R)-1-(4-Fluorophenyl)ethanol
This chemical is primarily used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds. Its chiral nature makes it valuable for creating enantiomerically pure drugs, which are essential for ensuring specific biological activity and reducing side effects. It is often employed in the development of antidepressants, antipsychotics, and other central nervous system (CNS) drugs. Additionally, it serves as a building block in organic synthesis for creating complex molecules with potential therapeutic applications. Its fluorine atom enhances the stability and bioavailability of the resulting compounds, making it a key component in medicinal chemistry research.
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