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

≥99%

Reagent Code: #92771
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CAS Number 53531-34-3

science Other reagents with same CAS 53531-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.26 g/mol
Formula C₁₆H₁₁F₃O
badge Registry Numbers
MDL Number MFCD00001260
thermostat Physical Properties
Melting Point 134-136°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used as a chiral resolving agent in asymmetric synthesis. It is effective in the separation of enantiomers, particularly in the pharmaceutical industry, where the production of single-enantiomer drugs is crucial for efficacy and safety. Additionally, it serves as a chiral shift reagent in nuclear magnetic resonance (NMR) spectroscopy, aiding in the determination of the enantiomeric purity of compounds. Its application extends to the field of organic chemistry, where it is employed in the synthesis of complex molecules with high stereochemical control.

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Test Parameter Specification
Appearance Yellow powder or crystals
Purity 98.5-100
Specific Rotation [α]^{20}_D (c=6, CHCl3) -28.0 to -22.0 deg
Solubility 50 mg/ml CHCl3: Clear, Yellow
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,360.00
inventory 10mg
10-20 days ฿2,440.00

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(R)-(-)-2,2,2-Trifluoro-1-(9-anthryl)ethanol
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This compound is primarily used as a chiral resolving agent in asymmetric synthesis. It is effective in the separation of enantiomers, particularly in the pharmaceutical industry, where the production of single-enantiomer drugs is crucial for efficacy and safety. Additionally, it serves as a chiral shift reagent in nuclear magnetic resonance (NMR) spectroscopy, aiding in the determination of the enantiomeric purity of compounds. Its application extends to the field of organic chemistry, where it is employed in the synthesis of complex molecules with high stereochemical control.
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