(R)-1-[(Sp)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenylethyldi-tert-butylphosphine

98%

Reagent Code: #228646
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CAS Number 1093686-50-0

science Other reagents with same CAS 1093686-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 652.58 g/mol
Formula C₃₈H₅₂FeO₂P₂
badge Registry Numbers
MDL Number MFCD08561156
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 pharmaceutical intermediates, where high enantiomeric excess is required. Its sterically bulky and electron-rich phosphine groups enhance catalytic activity and selectivity when paired with transition metals like rhodium or ruthenium. Common applications include the production of fine chemicals, agrochemicals, and active pharmaceutical ingredients where precise stereochemistry is critical. The ferrocene backbone provides structural rigidity and stability, supporting consistent performance under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,490.00
inventory 250mg
10-20 days ฿11,010.00
inventory 1g
10-20 days ฿29,650.00

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(R)-1-[(Sp)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenylethyldi-tert-butylphosphine
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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 pharmaceutical intermediates, where high enantiomeric excess is required. Its sterically bulky and electron-rich phosphine groups enhance catalytic activity and selectivity when paired with transition metals like rhodium or ruthenium. Common applications include the production of fine chemicals, agrochemicals, and activ

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 pharmaceutical intermediates, where high enantiomeric excess is required. Its sterically bulky and electron-rich phosphine groups enhance catalytic activity and selectivity when paired with transition metals like rhodium or ruthenium. Common applications include the production of fine chemicals, agrochemicals, and active pharmaceutical ingredients where precise stereochemistry is critical. The ferrocene backbone provides structural rigidity and stability, supporting consistent performance under various reaction conditions.

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