(S)-()-α-Methoxy-α-trifluoromethylphenylacetyl chloride

99%

Reagent Code: #113881
label
Alias (s)-(+)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride
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CAS Number 20445-33-4

science Other reagents with same CAS 20445-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.62 g/mol
Formula C₁₀H₈ClF₃O₂
badge Registry Numbers
MDL Number MFCD00067105
thermostat Physical Properties
Boiling Point 213-214 °C(lit.)
inventory_2 Storage & Handling
Density 1.35 g/mL at 25 °C(lit.)
Storage -20°C, dry

description Product Description

This chemical is widely used as a chiral derivatizing agent in organic synthesis, particularly for the resolution of enantiomers in racemic mixtures. It reacts with alcohols, amines, and other nucleophiles to form diastereomers, which can then be separated and analyzed using techniques like chromatography or spectroscopy. Its application is crucial in the pharmaceutical industry for the synthesis and purification of enantiomerically pure compounds, ensuring the desired biological activity and reducing potential side effects. Additionally, it serves as a key reagent in the preparation of chiral intermediates for agrochemicals and fine chemicals.

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Test Parameter Specification
Purity (GC) 98.5-100
Refractive Index (N20/D) 1.467-1.47
Specific Rotation [A]20/D (C=2, Toluene) 145-152
Appearance Colorless To Light Yellow Liquid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,600.00
inventory 100mg
10-20 days ฿6,990.00
inventory 250mg
10-20 days ฿16,600.00

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(S)-()-α-Methoxy-α-trifluoromethylphenylacetyl chloride
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This chemical is widely used as a chiral derivatizing agent in organic synthesis, particularly for the resolution of enantiomers in racemic mixtures. It reacts with alcohols, amines, and other nucleophiles to form diastereomers, which can then be separated and analyzed using techniques like chromatography or spectroscopy. Its application is crucial in the pharmaceutical industry for the synthesis and purification of enantiomerically pure compounds, ensuring the desired biological activity and reducing po

This chemical is widely used as a chiral derivatizing agent in organic synthesis, particularly for the resolution of enantiomers in racemic mixtures. It reacts with alcohols, amines, and other nucleophiles to form diastereomers, which can then be separated and analyzed using techniques like chromatography or spectroscopy. Its application is crucial in the pharmaceutical industry for the synthesis and purification of enantiomerically pure compounds, ensuring the desired biological activity and reducing potential side effects. Additionally, it serves as a key reagent in the preparation of chiral intermediates for agrochemicals and fine chemicals.

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