(4S,4'S)-4,4'-Diisopropyl-1,1'-di-m-tolyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole

97%

Reagent Code: #236866
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CAS Number 2374958-85-5

science Other reagents with same CAS 2374958-85-5

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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 stereogenic centers make it effective in coordinating transition metals like copper or nickel, enabling high enantioselectivity in reactions such as conjugate additions and cyclopropanations. The isopropyl and m-tolyl groups enhance steric and electronic tuning, improving selectivity and catalyst stability. Commonly applied in pharmaceutical synthesis where precise stereochemistry is critical.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿10,420.00
inventory 250mg
10-20 days ฿21,850.00
inventory 1g
10-20 days ฿67,050.00
inventory 100mg
10-20 days ฿14,570.00

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(4S,4'S)-4,4'-Diisopropyl-1,1'-di-m-tolyl-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 stereogenic centers make it effective in coordinating transition metals like copper or nickel, enabling high enantioselectivity in reactions such as conjugate additions and cyclopropanations. The isopropyl and m-tolyl groups enhance steric and electronic tuning, improving selectivity and catalyst stability. Commonly applied in pharmaceutical synthesis where precise st
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid biimidazole backbone and stereogenic centers make it effective in coordinating transition metals like copper or nickel, enabling high enantioselectivity in reactions such as conjugate additions and cyclopropanations. The isopropyl and m-tolyl groups enhance steric and electronic tuning, improving selectivity and catalyst stability. Commonly applied in pharmaceutical synthesis where precise stereochemistry is critical.
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