(S)-()-2,2,2-Trifluoro-1-(9-anthryl)ethanol

≥99%

Reagent Code: #92772
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CAS Number 60646-30-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.26 g/mol
Formula C₁₆H₁₁F₃O
badge Registry Numbers
MDL Number MFCD00062968
thermostat Physical Properties
Melting Point 134-136°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is widely used as a chiral resolving agent in organic synthesis. It is particularly effective in the separation of enantiomers, which is crucial in the production of pharmaceuticals where the biological activity of a compound often depends on its chirality. The anthryl group in the compound enhances its ability to form diastereomeric complexes with other chiral molecules, facilitating their separation through methods like crystallization or chromatography. Additionally, it serves as a chiral shift reagent in NMR spectroscopy, helping to distinguish between enantiomers in a mixture by inducing different chemical shifts for each enantiomer. This property is valuable in the analysis and quality control of chiral drugs and other enantiomerically pure substances.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 99-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days Ft81,596.77
(S)-()-2,2,2-Trifluoro-1-(9-anthryl)ethanol
This chemical is widely used as a chiral resolving agent in organic synthesis. It is particularly effective in the separation of enantiomers, which is crucial in the production of pharmaceuticals where the biological activity of a compound often depends on its chirality. The anthryl group in the compound enhances its ability to form diastereomeric complexes with other chiral molecules, facilitating their separation through methods like crystallization or chromatography. Additionally, it serves as a chiral shift reagent in NMR spectroscopy, helping to distinguish between enantiomers in a mixture by inducing different chemical shifts for each enantiomer. This property is valuable in the analysis and quality control of chiral drugs and other enantiomerically pure substances.
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