1,2-Ethanediamine, 1,2-bis(2-chlorophenyl)-, (1R,2R)-

97%(HPLC), 99%ee

Reagent Code: #229170
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CAS Number 1055703-96-2

science Other reagents with same CAS 1055703-96-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.18 g/mol
Formula C₁₄H₁₄Cl₂N₂
thermostat Physical Properties
Boiling Point 404.3±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.303±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a chiral ligand in asymmetric synthesis, this compound plays a key role in catalyzing enantioselective reactions. Its rigid structure and stereochemistry make it valuable in the development of pharmaceutical intermediates where high enantiomeric purity is required. It is also employed in coordination chemistry to form stable complexes with transition metals, which are then used as catalysts in hydrogenation and other transformation reactions. Due to its ability to influence stereochemical outcomes, it finds application in research and development of fine chemicals and active pharmaceutical ingredients.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,890.00
500mg
10-20 days ฿36,290.00
1,2-Ethanediamine, 1,2-bis(2-chlorophenyl)-, (1R,2R)-
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Used primarily as a chiral ligand in asymmetric synthesis, this compound plays a key role in catalyzing enantioselective reactions. Its rigid structure and stereochemistry make it valuable in the development of pharmaceutical intermediates where high enantiomeric purity is required. It is also employed in coordination chemistry to form stable complexes with transition metals, which are then used as catalysts in hydrogenation and other transformation reactions. Due to its ability to influence stereochemic

Used primarily as a chiral ligand in asymmetric synthesis, this compound plays a key role in catalyzing enantioselective reactions. Its rigid structure and stereochemistry make it valuable in the development of pharmaceutical intermediates where high enantiomeric purity is required. It is also employed in coordination chemistry to form stable complexes with transition metals, which are then used as catalysts in hydrogenation and other transformation reactions. Due to its ability to influence stereochemical outcomes, it finds application in research and development of fine chemicals and active pharmaceutical ingredients.

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