(2R)-1-[(S)-α-(Dimethylamino)-2-(diphenylphosphino)benzyl]-2-diphenylphosphinoferrocene

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Reagent Code: #230587
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CAS Number 850444-36-9

science Other reagents with same CAS 850444-36-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 687.57 g/mol
Formula C₄₃H₃₉FeNP₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in hydrogenation reactions, particularly for the enantioselective reduction of prochiral olefins and ketones. It is especially effective in the synthesis of chiral pharmaceutical intermediates and fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, enhancing catalytic performance in transition metal complexes, notably with rhodium and ruthenium. The presence of two phosphine groups and a stereogenic center allows for precise control over stereochemistry in the product, making it valuable in academic research and industrial asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,500.00
inventory 100mg
10-20 days ฿2,120.00
inventory 250mg
10-20 days ฿4,890.00
inventory 1g
10-20 days ฿17,200.00

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(2R)-1-[(S)-α-(Dimethylamino)-2-(diphenylphosphino)benzyl]-2-diphenylphosphinoferrocene
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in hydrogenation reactions, particularly for the enantioselective reduction of prochiral olefins and ketones. It is especially effective in the synthesis of chiral pharmaceutical intermediates and fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, enhancing catalytic performance in transition metal complexes, notably with rhodium and ruthenium.

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in hydrogenation reactions, particularly for the enantioselective reduction of prochiral olefins and ketones. It is especially effective in the synthesis of chiral pharmaceutical intermediates and fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, enhancing catalytic performance in transition metal complexes, notably with rhodium and ruthenium. The presence of two phosphine groups and a stereogenic center allows for precise control over stereochemistry in the product, making it valuable in academic research and industrial asymmetric synthesis.

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