(S)-1-(Anthracen-2-yl)propan-1-amine hydrochloride

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Reagent Code: #233247
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CAS Number 2703746-38-5

science Other reagents with same CAS 2703746-38-5

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scatter_plot Molecular Information
Weight 271.78 g/mol
Formula C₁₇H₁₈ClN
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MDL Number MFCD34186989
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral derivatizing agent in the analysis of enantiomeric purity, particularly in stereoselective synthesis and pharmaceutical research. Its anthracene moiety allows for strong UV and fluorescence detection, making it valuable in high-performance liquid chromatography (HPLC) for separating and quantifying enantiomers. Commonly employed in the development and quality control of chiral drugs where precise stereochemical determination is critical. Also serves as a building block in asymmetric synthesis for creating bioactive molecules with defined stereochemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,580.00
inventory 250mg
10-20 days ฿30,780.00

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(S)-1-(Anthracen-2-yl)propan-1-amine hydrochloride
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Used as a chiral derivatizing agent in the analysis of enantiomeric purity, particularly in stereoselective synthesis and pharmaceutical research. Its anthracene moiety allows for strong UV and fluorescence detection, making it valuable in high-performance liquid chromatography (HPLC) for separating and quantifying enantiomers. Commonly employed in the development and quality control of chiral drugs where precise stereochemical determination is critical. Also serves as a building block in asymmetric synt

Used as a chiral derivatizing agent in the analysis of enantiomeric purity, particularly in stereoselective synthesis and pharmaceutical research. Its anthracene moiety allows for strong UV and fluorescence detection, making it valuable in high-performance liquid chromatography (HPLC) for separating and quantifying enantiomers. Commonly employed in the development and quality control of chiral drugs where precise stereochemical determination is critical. Also serves as a building block in asymmetric synthesis for creating bioactive molecules with defined stereochemistry.

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