(4S,4'S)-4,4'-Diisopropyl-1,1'-bis(4-methoxyphenyl)-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole

97%

Reagent Code: #236864
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CAS Number 2374958-83-3

science Other reagents with same CAS 2374958-83-3

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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 transformations such as hydrogenation and transfer hydrogenation reactions. Its stereochemistry enables high enantioselectivity when coordinating with transition metals like ruthenium, rhodium, or iridium. Commonly applied in the synthesis of chiral amines, alcohols, and other fine chemicals important in pharmaceutical and agrochemical industries. Also employed in organocatalytic systems due to its ability to form stable hydrogen-bonded complexes with substrates, facilitating stereocontrol in bond-forming reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,300.00
inventory 250mg
10-20 days ฿19,060.00
inventory 1g
10-20 days ฿66,600.00

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(4S,4'S)-4,4'-Diisopropyl-1,1'-bis(4-methoxyphenyl)-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 transformations such as hydrogenation and transfer hydrogenation reactions. Its stereochemistry enables high enantioselectivity when coordinating with transition metals like ruthenium, rhodium, or iridium. Commonly applied in the synthesis of chiral amines, alcohols, and other fine chemicals important in pharmaceutical and agrochemical industries. Also employed in organocatalytic systems due to its ability to form stable hy

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation and transfer hydrogenation reactions. Its stereochemistry enables high enantioselectivity when coordinating with transition metals like ruthenium, rhodium, or iridium. Commonly applied in the synthesis of chiral amines, alcohols, and other fine chemicals important in pharmaceutical and agrochemical industries. Also employed in organocatalytic systems due to its ability to form stable hydrogen-bonded complexes with substrates, facilitating stereocontrol in bond-forming reactions.

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