(4R,4'R)-1,1'-Bis(3-(tert-butyl)phenyl)-4,4'-dicyclohexyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole

98%

Reagent Code: #232047
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CAS Number 2770054-34-5

science Other reagents with same CAS 2770054-34-5

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Weight 566.86 g/mol
Formula C₃₈H₅₄N₄
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Storage Room temperature

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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and transfer hydrogenation reactions. Its sterically hindered structure enhances selectivity and stability in metal-catalyzed processes, making it valuable in pharmaceutical synthesis where high enantiomeric purity is required. Also employed in the development of chiral catalysts for carbon-carbon bond-forming reactions, contributing to efficient and selective synthesis of complex molecules.

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inventory 100mg
10-20 days ฿9,600.00

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(4R,4'R)-1,1'-Bis(3-(tert-butyl)phenyl)-4,4'-dicyclohexyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and transfer hydrogenation reactions. Its sterically hindered structure enhances selectivity and stability in metal-catalyzed processes, making it valuable in pharmaceutical synthesis where high enantiomeric purity is required. Also employed in the development of chiral catalysts for carbon-carbon bond-forming reactions, contributing to efficient and selective synthesis of complex
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and transfer hydrogenation reactions. Its sterically hindered structure enhances selectivity and stability in metal-catalyzed processes, making it valuable in pharmaceutical synthesis where high enantiomeric purity is required. Also employed in the development of chiral catalysts for carbon-carbon bond-forming reactions, contributing to efficient and selective synthesis of complex molecules.
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