N-[(1S)-1-[3',5'-Bis(1,1-dimethylethyl)[1,1'-biphenyl]-2-yl]-2-(diphenylphosphino)ethyl]-3,5-bis(trifluoromethyl)-benzamide

98%

Reagent Code: #68818
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CAS Number 2089424-11-1

science Other reagents with same CAS 2089424-11-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 733.8 g/mol
Formula C₄₃H₄₂F₆NOP
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used as a ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring bulky tert-butyl groups and electron-withdrawing trifluoromethyl groups, makes it highly effective in controlling stereochemistry during catalytic processes. It is often employed in the synthesis of chiral compounds, such as pharmaceuticals and fine chemicals, where high enantioselectivity is crucial. The diphenylphosphino group enhances its ability to coordinate with metals, facilitating the formation of stable and active catalytic complexes. Its application is particularly notable in hydrogenation, cross-coupling, and other asymmetric transformations, contributing to the production of optically pure substances.

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Test Parameter Specification
Appearance Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 10mg
10-20 days ฿2,880.00

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N-[(1S)-1-[3',5'-Bis(1,1-dimethylethyl)[1,1'-biphenyl]-2-yl]-2-(diphenylphosphino)ethyl]-3,5-bis(trifluoromethyl)-benzamide
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This chemical is primarily used as a ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring bulky tert-butyl groups and electron-withdrawing trifluoromethyl groups, makes it highly effective in controlling stereochemistry during catalytic processes. It is often employed in the synthesis of chiral compounds, such as pharmaceuticals and fine chemicals, where high enantioselectivity is crucial. The diphenylphosphino group enhances its ability to

This chemical is primarily used as a ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring bulky tert-butyl groups and electron-withdrawing trifluoromethyl groups, makes it highly effective in controlling stereochemistry during catalytic processes. It is often employed in the synthesis of chiral compounds, such as pharmaceuticals and fine chemicals, where high enantioselectivity is crucial. The diphenylphosphino group enhances its ability to coordinate with metals, facilitating the formation of stable and active catalytic complexes. Its application is particularly notable in hydrogenation, cross-coupling, and other asymmetric transformations, contributing to the production of optically pure substances.

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