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

95%

Reagent Code: #236927
fingerprint
CAS Number 2828440-25-9

science Other reagents with same CAS 2828440-25-9

blur_circular Chemical Specifications

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

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its sterically hindered structure and defined stereochemistry make it effective in inducing high enantioselectivity when coordinating with transition metals like ruthenium, rhodium, or iridium. Commonly employed in the synthesis of chiral amines, alcohols, and other fine chemicals important in pharmaceutical and agrochemical industries. Also finds use in organocatalytic transformations due to its stable imidazolidine core and tunable electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,760.00
inventory 100mg
10-20 days ฿9,800.00
inventory 250mg
10-20 days ฿19,530.00
inventory 1g
10-20 days ฿67,900.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4S,4'S)-1,1'-Bis(3-(tert-butyl)phenyl)-4,4'-diisobutyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
No image available
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its sterically hindered structure and defined stereochemistry make it effective in inducing high enantioselectivity when coordinating with transition metals like ruthenium, rhodium, or iridium. Commonly employed in the synthesis of chiral amines, alcohols, and other fine chemicals important in pharmaceutical and agrochemical industries. Also finds use in organocatalytic trans
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its sterically hindered structure and defined stereochemistry make it effective in inducing high enantioselectivity when coordinating with transition metals like ruthenium, rhodium, or iridium. Commonly employed in the synthesis of chiral amines, alcohols, and other fine chemicals important in pharmaceutical and agrochemical industries. Also finds use in organocatalytic transformations due to its stable imidazolidine core and tunable electronic properties.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...