(S)-1-(Anthracen-9-yl)-2,2,2-trifluoroethan-1-amine hydrochloride

95%

Reagent Code: #236944
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CAS Number 336105-49-8

science Other reagents with same CAS 336105-49-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.7293 g/mol
Formula C₁₆H₁₃ClF₃N
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral derivatizing agent in the analysis of enantiomeric purity, particularly in NMR spectroscopy. Its anthracene moiety provides a strong chromophore, enabling sensitive detection in UV-based analytical methods. Commonly employed to resolve and quantify enantiomers of chiral carboxylic acids and other acidic compounds through diastereomeric amide formation. Also applied in asymmetric synthesis as a chiral auxiliary or intermediate in the preparation of fluorinated bioactive molecules. The trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable in pharmaceutical research for developing CNS-active agents and other therapeutic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,750.00
inventory 250mg
10-20 days ฿36,200.00

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(S)-1-(Anthracen-9-yl)-2,2,2-trifluoroethan-1-amine hydrochloride
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Used as a chiral derivatizing agent in the analysis of enantiomeric purity, particularly in NMR spectroscopy. Its anthracene moiety provides a strong chromophore, enabling sensitive detection in UV-based analytical methods. Commonly employed to resolve and quantify enantiomers of chiral carboxylic acids and other acidic compounds through diastereomeric amide formation. Also applied in asymmetric synthesis as a chiral auxiliary or intermediate in the preparation of fluorinated bioactive molecules. The tri

Used as a chiral derivatizing agent in the analysis of enantiomeric purity, particularly in NMR spectroscopy. Its anthracene moiety provides a strong chromophore, enabling sensitive detection in UV-based analytical methods. Commonly employed to resolve and quantify enantiomers of chiral carboxylic acids and other acidic compounds through diastereomeric amide formation. Also applied in asymmetric synthesis as a chiral auxiliary or intermediate in the preparation of fluorinated bioactive molecules. The trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable in pharmaceutical research for developing CNS-active agents and other therapeutic compounds.

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