(1R,2R)-1,2-di([1,1'-biphenyl]-2-yl)ethane-1,2-diamine

97%(HPLC), 99%ee

Reagent Code: #229167
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CAS Number 2380225-24-9

science Other reagents with same CAS 2380225-24-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 364.49 g/mol
Formula C₂₆H₂₄N₂
thermostat Physical Properties
Boiling Point 578.3±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.130±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective synthesis, particularly in hydrogenation and transfer hydrogenation reactions. It is effective in the preparation of chiral amines and alcohols, which are important intermediates in pharmaceuticals. Due to its rigid biphenyl structure and defined stereochemistry, it provides high enantioselectivity when coordinated with metals like ruthenium, rhodium, or iridium. It is especially valuable in the synthesis of biologically active molecules where control of stereochemistry is critical.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿10,990.00
inventory 100mg
10-20 days ฿32,990.00

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(1R,2R)-1,2-di([1,1'-biphenyl]-2-yl)ethane-1,2-diamine
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective synthesis, particularly in hydrogenation and transfer hydrogenation reactions. It is effective in the preparation of chiral amines and alcohols, which are important intermediates in pharmaceuticals. Due to its rigid biphenyl structure and defined stereochemistry, it provides high enantioselectivity when coordinated with metals like ruthenium, rhodium, or iridium. It is especially valuable in the syn

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective synthesis, particularly in hydrogenation and transfer hydrogenation reactions. It is effective in the preparation of chiral amines and alcohols, which are important intermediates in pharmaceuticals. Due to its rigid biphenyl structure and defined stereochemistry, it provides high enantioselectivity when coordinated with metals like ruthenium, rhodium, or iridium. It is especially valuable in the synthesis of biologically active molecules where control of stereochemistry is critical.

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