(1S, 2S)-1,2-di-1-Naphthyl-ethylenediaMine dihydrochloride

97%

Reagent Code: #235892
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CAS Number 1052707-27-3

science Other reagents with same CAS 1052707-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 385.33 g/mol
Formula C₂₂H₂₂Cl₂N₂
badge Registry Numbers
MDL Number MFCD09836226
thermostat Physical Properties
Melting Point 219-224°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid naphthyl groups provide steric bulk and π-π interactions that enhance stereocontrol in reactions such as asymmetric transfer hydrogenation of ketones and imines. Commonly employed with ruthenium, rhodium, or iridium metal centers to form catalytically active complexes. Valued for high enantioselectivity in the synthesis of chiral alcohols and amines, which are key intermediates in pharmaceuticals and fine chemicals. Soluble in polar organic solvents, making it suitable for homogeneous catalytic systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,460.00
(1S, 2S)-1,2-di-1-Naphthyl-ethylenediaMine dihydrochloride
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid naphthyl groups provide steric bulk and π-π interactions that enhance stereocontrol in reactions such as asymmetric transfer hydrogenation of ketones and imines. Commonly employed with ruthenium, rhodium, or iridium metal centers to form catalytically active complexes. Valued for high enantioselectivity in the synthesis of chiral alcohols and amines, which are key intermediates in pharmace

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid naphthyl groups provide steric bulk and π-π interactions that enhance stereocontrol in reactions such as asymmetric transfer hydrogenation of ketones and imines. Commonly employed with ruthenium, rhodium, or iridium metal centers to form catalytically active complexes. Valued for high enantioselectivity in the synthesis of chiral alcohols and amines, which are key intermediates in pharmaceuticals and fine chemicals. Soluble in polar organic solvents, making it suitable for homogeneous catalytic systems.

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