(4S,4'S)-1,1'-Di([1,1'-biphenyl]-4-yl)-4,4'-diisopropyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole

97%

Reagent Code: #236867
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CAS Number 2374958-86-6

science Other reagents with same CAS 2374958-86-6

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and C–C bond formation reactions. Its rigid, chiral biimidazole framework enhances stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Soluble in common organic solvents, it is compatible with transition metal complexes like ruthenium or rhodium, improving catalytic efficiency and enantioselectivity. Also applied in research for developing chiral sensors and asymmetric synthesis methodologies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,320.00
inventory 250mg
10-20 days ฿13,120.00
inventory 1g
10-20 days ฿47,910.00

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(4S,4'S)-1,1'-Di([1,1'-biphenyl]-4-yl)-4,4'-diisopropyl-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 C–C bond formation reactions. Its rigid, chiral biimidazole framework enhances stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Soluble in common organic solvents, it is compatible with transition metal complexes like ruthenium or rhodium, improving catalytic efficiency and enantioselectivity. Also applied in research

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and C–C bond formation reactions. Its rigid, chiral biimidazole framework enhances stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Soluble in common organic solvents, it is compatible with transition metal complexes like ruthenium or rhodium, improving catalytic efficiency and enantioselectivity. Also applied in research for developing chiral sensors and asymmetric synthesis methodologies.

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