Bis[(S)-1-phenylethyl]amine

≥98%

Reagent Code: #149269
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CAS Number 56210-72-1

science Other reagents with same CAS 56210-72-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.34 g/mol
Formula C₁₆H₁₉N
badge Registry Numbers
MDL Number MFCD00243087
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral auxiliary and resolving agent in asymmetric synthesis, particularly in the preparation of enantiomerically pure amines and amino derivatives. Its stereoselective properties make it valuable in pharmaceutical intermediates synthesis where chirality affects biological activity. Commonly employed in the resolution of racemic mixtures through diastereomeric salt formation, enabling separation of enantiomers. Also utilized in catalysis and as a building block for chiral ligands in enantioselective transformations.

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Test Parameter Specification
Appearance Colorless to light yellow liquid
Purity (%) 98-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿390.00
inventory 1g
10-20 days ฿1,050.00
inventory 5g
10-20 days ฿3,740.00
inventory 25g
10-20 days ฿17,000.00

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Bis[(S)-1-phenylethyl]amine
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Used as a chiral auxiliary and resolving agent in asymmetric synthesis, particularly in the preparation of enantiomerically pure amines and amino derivatives. Its stereoselective properties make it valuable in pharmaceutical intermediates synthesis where chirality affects biological activity. Commonly employed in the resolution of racemic mixtures through diastereomeric salt formation, enabling separation of enantiomers. Also utilized in catalysis and as a building block for chiral ligands in enantiosele

Used as a chiral auxiliary and resolving agent in asymmetric synthesis, particularly in the preparation of enantiomerically pure amines and amino derivatives. Its stereoselective properties make it valuable in pharmaceutical intermediates synthesis where chirality affects biological activity. Commonly employed in the resolution of racemic mixtures through diastereomeric salt formation, enabling separation of enantiomers. Also utilized in catalysis and as a building block for chiral ligands in enantioselective transformations.

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