(1R,1'R)-1,1',2,2',3,3',4,4'-Octahydro-1,1'-biisoquinoline

97% 99%ee

Reagent Code: #231464
fingerprint
CAS Number 634180-49-7

science Other reagents with same CAS 634180-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.36 g/mol
Formula C₁₈H₂₀N₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid, C2-symmetric structure enhances stereocontrol, making it valuable in the synthesis of chiral amines and pharmaceutical intermediates. Commonly employed in ruthenium- or rhodium-catalyzed systems for high enantioselectivity. Also applied in the development of catalysts for fine chemicals and active pharmaceutical ingredients (APIs) where precise stereochemistry is critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,150.00
inventory 250mg
10-20 days ฿16,900.00
inventory 1g
10-20 days ฿56,660.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(1R,1'R)-1,1',2,2',3,3',4,4'-Octahydro-1,1'-biisoquinoline
No image available

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid, C2-symmetric structure enhances stereocontrol, making it valuable in the synthesis of chiral amines and pharmaceutical intermediates. Commonly employed in ruthenium- or rhodium-catalyzed systems for high enantioselectivity. Also applied in the development of catalysts for fine chemicals and active pharmaceutical ingredients (APIs) where precise stereochemistry i

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation and transfer hydrogenation reactions. Its rigid, C2-symmetric structure enhances stereocontrol, making it valuable in the synthesis of chiral amines and pharmaceutical intermediates. Commonly employed in ruthenium- or rhodium-catalyzed systems for high enantioselectivity. Also applied in the development of catalysts for fine chemicals and active pharmaceutical ingredients (APIs) where precise stereochemistry is critical.

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...