2-(Diphenylphosphino)-N-((S)-((1S, 2S, 4S, 5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)benzamide

98%

Reagent Code: #177922
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CAS Number 1630973-06-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 613.73 g/mol
Formula C₃₉H₄₀N₃O₂P
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective hydrogenation reactions. It is particularly effective in the synthesis of chiral amines and amino acid derivatives, which are important intermediates in pharmaceutical manufacturing. Due to its rigid quinuclidine backbone and tunable phosphine moiety, it provides high enantioselectivity and catalytic efficiency when coordinated with transition metals such as rhodium or ruthenium. Its application is prominent in the production of active pharmaceutical ingredients (APIs) where control of stereochemistry is critical for biological activity. The compound enables greener processes by allowing lower catalyst loadings and milder reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days €275.74
inventory 100mg
10-20 days €412.02
inventory 250mg
10-20 days €618.17
2-(Diphenylphosphino)-N-((S)-((1S, 2S, 4S, 5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methyl)benzamide
Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective hydrogenation reactions. It is particularly effective in the synthesis of chiral amines and amino acid derivatives, which are important intermediates in pharmaceutical manufacturing. Due to its rigid quinuclidine backbone and tunable phosphine moiety, it provides high enantioselectivity and catalytic efficiency when coordinated with transition metals such as rhodium or ruthenium. Its application is prominent in the production of active pharmaceutical ingredients (APIs) where control of stereochemistry is critical for biological activity. The compound enables greener processes by allowing lower catalyst loadings and milder reaction conditions.
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