(1R,2R)-1,2-bis(2-methoxyphenyl)-N1,N2-dimethylethane-1,2-diamine

97%(HPLC), 99% e.e.

Reagent Code: #229158
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CAS Number 2444430-79-7

science Other reagents with same CAS 2444430-79-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.4 g/mol
Formula C₁₈H₂₄N₂O₂
thermostat Physical Properties
Boiling Point 433.2±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.061±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. Its structure enables high stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions such as asymmetric transfer hydrogenation and carbon-carbon bond-forming reactions. The ligand’s rigid framework and electron-donating methoxy groups enhance metal coordination and reaction selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,160.00
inventory 100mg
10-20 days ฿16,990.00
(1R,2R)-1,2-bis(2-methoxyphenyl)-N1,N2-dimethylethane-1,2-diamine
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Used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. Its structure enables high stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions such as asymmetric transfer hydrogenation and carbon-carbon bond-forming reactions. The ligand’s rigid framework and electron-donating methoxy groups enhance metal coordination and reaction selectivity.

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. Its structure enables high stereocontrol, making it valuable in the preparation of optically active pharmaceuticals and fine chemicals. Commonly employed in transition metal-catalyzed reactions such as asymmetric transfer hydrogenation and carbon-carbon bond-forming reactions. The ligand’s rigid framework and electron-donating methoxy groups enhance metal coordination and reaction selectivity.

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