(1R,2R)-1,2-Di(naphthalen-1-yl)ethane-1,2-diamine Dihydrochloride

98%(HPLC)(T)

Reagent Code: #231061
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CAS Number 1055301-17-1

science Other reagents with same CAS 1055301-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 385.336 g/mol
Formula C₂₂H₂₂Cl₂N₂
badge Registry Numbers
MDL Number MFCD09953698
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. Its rigid structure and well-defined stereochemistry make it effective in inducing high enantioselectivity in transformations such as hydrogenation and transfer hydrogenation of prochiral ketones and imines. Commonly employed in conjunction with transition metals like ruthenium or rhodium to form catalytically active complexes. Also applied in the development of chiral catalysts for pharmaceutical synthesis where control of stereochemistry is critical. Its dihydrochloride salt form enhances solubility and stability, facilitating handling and storage in industrial and laboratory settings.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,240.00
(1R,2R)-1,2-Di(naphthalen-1-yl)ethane-1,2-diamine Dihydrochloride
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Used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. Its rigid structure and well-defined stereochemistry make it effective in inducing high enantioselectivity in transformations such as hydrogenation and transfer hydrogenation of prochiral ketones and imines. Commonly employed in conjunction with transition metals like ruthenium or rhodium to form catalytically active complexes. Also applied in the development of chiral catalysts for pharmaceutical synth

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic enantioselective reactions. Its rigid structure and well-defined stereochemistry make it effective in inducing high enantioselectivity in transformations such as hydrogenation and transfer hydrogenation of prochiral ketones and imines. Commonly employed in conjunction with transition metals like ruthenium or rhodium to form catalytically active complexes. Also applied in the development of chiral catalysts for pharmaceutical synthesis where control of stereochemistry is critical. Its dihydrochloride salt form enhances solubility and stability, facilitating handling and storage in industrial and laboratory settings.

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