(S)-1-(2-(Trifluoromethyl)phenyl)ethanol

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Reagent Code: #53066
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CAS Number 127852-27-1

science Other reagents with same CAS 127852-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.1600 g/mol
Formula C₉H₉OF₃
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MDL Number MFCD03093001
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a trifluoromethyl group, enhances the biological activity and metabolic stability of the final drug molecules. It is particularly valuable in the development of enantiomerically pure drugs, where the (S)-configuration plays a critical role in achieving the desired therapeutic effect. Additionally, it finds applications in organic synthesis as a building block for creating complex molecules with specific stereochemistry, often employed in the production of agrochemicals and specialty chemicals. Its unique properties make it a versatile reagent in asymmetric synthesis and catalysis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿666.00

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(S)-1-(2-(Trifluoromethyl)phenyl)ethanol
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This compound is primarily used in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a trifluoromethyl group, enhances the biological activity and metabolic stability of the final drug molecules. It is particularly valuable in the development of enantiomerically pure drugs, where the (S)-configuration plays a critical role in achieving the desired therapeutic effect. Additionally, it finds applications in or

This compound is primarily used in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a trifluoromethyl group, enhances the biological activity and metabolic stability of the final drug molecules. It is particularly valuable in the development of enantiomerically pure drugs, where the (S)-configuration plays a critical role in achieving the desired therapeutic effect. Additionally, it finds applications in organic synthesis as a building block for creating complex molecules with specific stereochemistry, often employed in the production of agrochemicals and specialty chemicals. Its unique properties make it a versatile reagent in asymmetric synthesis and catalysis.

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