(2S)-1-[(4R)-4,5-Dihydro-4-(1-methylethyl)-2-oxazolyl]-2-(diphenylphosphino)ferrocene

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Reagent Code: #36509
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CAS Number 1065474-88-5

science Other reagents with same CAS 1065474-88-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 481.3600 g/mol
Formula C₂₈H₂₈FeNOP
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a ferrocene backbone and a phosphine group, makes it an effective ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. It is especially valued in the pharmaceutical industry for producing enantiomerically pure compounds, which are crucial for drug development. Additionally, its stability and selectivity make it a preferred choice in academic and industrial research for exploring new catalytic processes.

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inventory 100mg
10-20 days ฿2,178.00

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(2S)-1-[(4R)-4,5-Dihydro-4-(1-methylethyl)-2-oxazolyl]-2-(diphenylphosphino)ferrocene
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This compound is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a ferrocene backbone and a phosphine group, makes it an effective ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. It is especially valued in the pharmaceutical industry for producing enantiomerically pure compounds, which are crucial for drug development. Additionally, its stability and selectivity

This compound is primarily utilized in asymmetric catalysis, particularly in the synthesis of chiral molecules. Its unique structure, featuring a ferrocene backbone and a phosphine group, makes it an effective ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. It is especially valued in the pharmaceutical industry for producing enantiomerically pure compounds, which are crucial for drug development. Additionally, its stability and selectivity make it a preferred choice in academic and industrial research for exploring new catalytic processes.

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