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

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Reagent Code: #236994
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CAS Number 634180-45-3

science Other reagents with same CAS 634180-45-3

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 synthesis, particularly in catalytic reactions where high enantioselectivity is required. Its rigid, bidentate structure makes it effective in coordinating with transition metals such as palladium, rhodium, and ruthenium, enabling efficient stereocontrol in hydrogenation, coupling, and cyclization reactions. Commonly applied in pharmaceutical research for the development of enantiomerically pure compounds. Also utilized in the design of catalysts for fine chemical production due to its stability under various reaction conditions.

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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

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(1S,1'S)-1,1',2,2',3,3',4,4'-Octahydro-1,1'-biisoquinoline
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Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. Its rigid, bidentate structure makes it effective in coordinating with transition metals such as palladium, rhodium, and ruthenium, enabling efficient stereocontrol in hydrogenation, coupling, and cyclization reactions. Commonly applied in pharmaceutical research for the development of enantiomerically pure compounds. Also utilized in the design of catalysts for fine chemical pr

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. Its rigid, bidentate structure makes it effective in coordinating with transition metals such as palladium, rhodium, and ruthenium, enabling efficient stereocontrol in hydrogenation, coupling, and cyclization reactions. Commonly applied in pharmaceutical research for the development of enantiomerically pure compounds. Also utilized in the design of catalysts for fine chemical production due to its stability under various reaction conditions.

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