(1R)-1-(Dicyclohexylphosphino)-2-[(S)-[2-(dicyclohexylphosphino)phenyl](dimethylamino)methyl]ferrocene

98%

Reagent Code: #230634
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CAS Number 914089-00-2

science Other reagents with same CAS 914089-00-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 711.76 g/mol
Formula C₄₃H₆₃FENP₂
badge Registry Numbers
MDL Number MFCD04117706
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 enantioselective hydrogenation reactions. It is particularly effective in the synthesis of chiral amines, amino acids, and other fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, while the phosphine groups coordinate efficiently with transition metals like rhodium and ruthenium, enhancing catalytic activity. Due to its tunable stereochemistry, it supports the development of pharmaceutical intermediates and agrochemicals where precise stereocontrol is critical. The ligand’s performance in homogeneous catalysis makes it valuable in both academic research and industrial processes focused on asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,160.00
inventory 1g
10-20 days ฿32,610.00

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(1R)-1-(Dicyclohexylphosphino)-2-[(S)-[2-(dicyclohexylphosphino)phenyl](dimethylamino)methyl]ferrocene
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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, amino acids, and other fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, while the phosphine groups coordinate efficiently with transition metals like rhodium and ruthenium, enhancing catalytic activity. Due to its tunable stereochemistr

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, amino acids, and other fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, while the phosphine groups coordinate efficiently with transition metals like rhodium and ruthenium, enhancing catalytic activity. Due to its tunable stereochemistry, it supports the development of pharmaceutical intermediates and agrochemicals where precise stereocontrol is critical. The ligand’s performance in homogeneous catalysis makes it valuable in both academic research and industrial processes focused on asymmetric synthesis.

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