(S)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetic acid

99%

Reagent Code: #234274
label
Alias (S)-(-)-α-methoxy-α-(trifluoromethyl)phenylacetic acid; S-methoxy-trifluoromethylphenylacetic acid
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CAS Number 17257-71-5

science Other reagents with same CAS 17257-71-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.17 g/mol
Formula C₁₀H₉F₃O₃
badge Registry Numbers
EC Number 241-292-1
MDL Number MFCD00064200
thermostat Physical Properties
Melting Point 46-49 °C(lit.)
Boiling Point 95-97 °C0.05 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.303 g/mL at 25 °C(lit.)
Storage 2~8°C, dry

description Product Description

Used as a chiral derivatizing agent in the resolution of enantiomers, particularly in the analysis of chiral alcohols and amines. Its ability to form diastereomeric esters or amides allows for separation by conventional chromatography or crystallization. Commonly employed in NMR spectroscopy to determine enantiomeric purity due to distinct chemical shifts of the resulting diastereomers. Also utilized in asymmetric synthesis and pharmaceutical development where stereochemical control is critical.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,400.00
inventory 250mg
10-20 days ฿5,190.00
inventory 1g
10-20 days ฿13,500.00
inventory 5g
10-20 days ฿46,990.00

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(S)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetic acid
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Used as a chiral derivatizing agent in the resolution of enantiomers, particularly in the analysis of chiral alcohols and amines. Its ability to form diastereomeric esters or amides allows for separation by conventional chromatography or crystallization. Commonly employed in NMR spectroscopy to determine enantiomeric purity due to distinct chemical shifts of the resulting diastereomers. Also utilized in asymmetric synthesis and pharmaceutical development where stereochemical control is critical.

Used as a chiral derivatizing agent in the resolution of enantiomers, particularly in the analysis of chiral alcohols and amines. Its ability to form diastereomeric esters or amides allows for separation by conventional chromatography or crystallization. Commonly employed in NMR spectroscopy to determine enantiomeric purity due to distinct chemical shifts of the resulting diastereomers. Also utilized in asymmetric synthesis and pharmaceutical development where stereochemical control is critical.

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