(1R,2R)-N1,N1-Dimethyl-1,2-diphenylethane-1,2-diamine dihydrochloride

97%

Reagent Code: #229285
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CAS Number 2635339-86-3

science Other reagents with same CAS 2635339-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.27 g/mol
Formula C₁₆H₂₂Cl₂N₂
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid backbone and well-defined stereochemistry make it effective in inducing high enantioselectivity when complexed with transition metals like ruthenium or rhodium. Commonly applied in the synthesis of chiral amines and pharmaceutical intermediates where stereochemical purity is critical. Also employed in the development of asymmetric C–C bond-forming reactions and in organocatalytic transformations due to its ability to form stable complexes with metal centers and influence reaction pathways through steric and electronic control.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,380.00
inventory 250mg
10-20 days ฿9,060.00
(1R,2R)-N1,N1-Dimethyl-1,2-diphenylethane-1,2-diamine dihydrochloride
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid backbone and well-defined stereochemistry make it effective in inducing high enantioselectivity when complexed with transition metals like ruthenium or rhodium. Commonly applied in the synthesis of chiral amines and pharmaceutical intermediates where stereochemical purity is critical. Also employed in the development of asymmetric C–C bond-forming reactions and i

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid backbone and well-defined stereochemistry make it effective in inducing high enantioselectivity when complexed with transition metals like ruthenium or rhodium. Commonly applied in the synthesis of chiral amines and pharmaceutical intermediates where stereochemical purity is critical. Also employed in the development of asymmetric C–C bond-forming reactions and in organocatalytic transformations due to its ability to form stable complexes with metal centers and influence reaction pathways through steric and electronic control.

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