(2S)-1-[(4S)-4,5-dihydro-4-phenyl-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene

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Reagent Code: #59666
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CAS Number 291536-01-1

science Other reagents with same CAS 291536-01-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 515.40 g/mol
Formula C₃₁H₂₆FeNOP
badge Registry Numbers
MDL Number MFCD30475631
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the field of organic chemistry. Its unique structure, featuring a ferrocene backbone and chiral oxazoline-phosphine ligands, makes it highly effective as a chiral ligand in transition metal-catalyzed reactions. It is commonly employed in asymmetric hydrogenation, a process critical for producing enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Additionally, it finds application in carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation, contributing to the development of complex organic molecules with high stereoselectivity. Its versatility and efficiency in promoting enantioselective transformations make it a valuable tool in synthetic organic chemistry.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,080.00
inventory 250mg
10-20 days ฿4,293.00

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(2S)-1-[(4S)-4,5-dihydro-4-phenyl-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene
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This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the field of organic chemistry. Its unique structure, featuring a ferrocene backbone and chiral oxazoline-phosphine ligands, makes it highly effective as a chiral ligand in transition metal-catalyzed reactions. It is commonly employed in asymmetric hydrogenation, a process critical for producing enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceu

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the field of organic chemistry. Its unique structure, featuring a ferrocene backbone and chiral oxazoline-phosphine ligands, makes it highly effective as a chiral ligand in transition metal-catalyzed reactions. It is commonly employed in asymmetric hydrogenation, a process critical for producing enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Additionally, it finds application in carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation, contributing to the development of complex organic molecules with high stereoselectivity. Its versatility and efficiency in promoting enantioselective transformations make it a valuable tool in synthetic organic chemistry.

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