(4S,4'S)-1,1',4,4'-Tetraisopropyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole

97%

Reagent Code: #236868
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CAS Number 2374958-87-7

science Other reagents with same CAS 2374958-87-7

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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. Its rigid biimidazole backbone and chiral environment make it effective in coordinating transition metals for catalytic reactions such as asymmetric hydrogenation and C–C bond formation. The isopropyl groups enhance steric hindrance, improving enantioselectivity. Commonly applied in pharmaceutical synthesis where high optical purity is required. Also investigated in organocatalysis due to its ability to form stable hydrogen-bonded complexes with substrates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,110.00
inventory 250mg
10-20 days ฿19,060.00
inventory 1g
10-20 days ฿66,600.00

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(4S,4'S)-1,1',4,4'-Tetraisopropyl-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. Its rigid biimidazole backbone and chiral environment make it effective in coordinating transition metals for catalytic reactions such as asymmetric hydrogenation and C–C bond formation. The isopropyl groups enhance steric hindrance, improving enantioselectivity. Commonly applied in pharmaceutical synthesis where high optical purity is required. Also investigated in organocatalysis due to its abilit

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid biimidazole backbone and chiral environment make it effective in coordinating transition metals for catalytic reactions such as asymmetric hydrogenation and C–C bond formation. The isopropyl groups enhance steric hindrance, improving enantioselectivity. Commonly applied in pharmaceutical synthesis where high optical purity is required. Also investigated in organocatalysis due to its ability to form stable hydrogen-bonded complexes with substrates.

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