rel-(1R,2R)-N1,N2-Dimethyl-N1,N2-bis(pyridin-2-ylmethyl)cyclohexane-1,2-diamine

98%

Reagent Code: #228939
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CAS Number 515124-12-6

science Other reagents with same CAS 515124-12-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.46 g/mol
Formula C₂₀H₂₈N₄
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation and transfer hydrogenation reactions. Its rigid cyclohexane backbone and pyridyl coordination sites enable strong metal binding, commonly with ruthenium, rhodium, or iridium, to form highly selective catalysts. These complexes are effective in producing enantiomerically enriched amines, alcohols, and other fine chemicals important in pharmaceutical synthesis. The ligand’s stereochemistry enhances facial selectivity in substrate approach, leading to high enantiomeric excess. It is also employed in C–C bond formation reactions and has shown utility in catalytic asymmetric synthesis of biologically active molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿12,770.00
250mg
10-20 days ฿21,690.00
rel-(1R,2R)-N1,N2-Dimethyl-N1,N2-bis(pyridin-2-ylmethyl)cyclohexane-1,2-diamine
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation and transfer hydrogenation reactions. Its rigid cyclohexane backbone and pyridyl coordination sites enable strong metal binding, commonly with ruthenium, rhodium, or iridium, to form highly selective catalysts. These complexes are effective in producing enantiomerically enriched amines, alcohols, and other fine chemicals important in pharmaceutical synthesis. The ligand’s stereochemistr

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation and transfer hydrogenation reactions. Its rigid cyclohexane backbone and pyridyl coordination sites enable strong metal binding, commonly with ruthenium, rhodium, or iridium, to form highly selective catalysts. These complexes are effective in producing enantiomerically enriched amines, alcohols, and other fine chemicals important in pharmaceutical synthesis. The ligand’s stereochemistry enhances facial selectivity in substrate approach, leading to high enantiomeric excess. It is also employed in C–C bond formation reactions and has shown utility in catalytic asymmetric synthesis of biologically active molecules.

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