(R)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride

99%

Reagent Code: #113879
label
Alias (R)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride; Methoxy-trifluoromethylphenylacetyl chloride
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CAS Number 39637-99-5

science Other reagents with same CAS 39637-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.62 g/mol
Formula C₁₀H₈ClF₃O₂
badge Registry Numbers
MDL Number MFCD00044400
thermostat Physical Properties
Boiling Point 99 °C /1.6kPa
inventory_2 Storage & Handling
Density 1.35 g/mL at 25 °C(lit.)
Storage -20°C, dry, inert gas

description Product Description

This chemical is widely used as a chiral derivatizing agent in organic synthesis and analytical chemistry. It is particularly valuable for the resolution and determination of enantiomeric purity of chiral compounds, such as alcohols, amines, and amino acids. By forming diastereomeric derivatives, it enables the separation and quantification of enantiomers using techniques like HPLC or NMR. Additionally, it serves as a key reagent in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals, where precise stereochemistry is critical for biological activity. Its trifluoromethyl group enhances reactivity and selectivity, making it a preferred choice in asymmetric synthesis and chiral analysis.

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Test Parameter Specification
Appearance Colorless to light yellow to yellow liquid
Purity (%) 98.5-100%
Specific Rotation [α]20/D (c=6.4 in Carbon Tetrachloride) -139.0 to -135.0
Tetrachloride -139.0--135.0°
Refractive Index (20°C, 589 nm) 1.4675-1.4715
Infrared Spectrum Conforms To Structure
NMR Conforms to structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,780.00

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(R)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride
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This chemical is widely used as a chiral derivatizing agent in organic synthesis and analytical chemistry. It is particularly valuable for the resolution and determination of enantiomeric purity of chiral compounds, such as alcohols, amines, and amino acids. By forming diastereomeric derivatives, it enables the separation and quantification of enantiomers using techniques like HPLC or NMR. Additionally, it serves as a key reagent in the synthesis of enantiomerically pure pharmaceuticals and fine chemical

This chemical is widely used as a chiral derivatizing agent in organic synthesis and analytical chemistry. It is particularly valuable for the resolution and determination of enantiomeric purity of chiral compounds, such as alcohols, amines, and amino acids. By forming diastereomeric derivatives, it enables the separation and quantification of enantiomers using techniques like HPLC or NMR. Additionally, it serves as a key reagent in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals, where precise stereochemistry is critical for biological activity. Its trifluoromethyl group enhances reactivity and selectivity, making it a preferred choice in asymmetric synthesis and chiral analysis.

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