(R)-2,2'-Bis[bis(4-methoxy-3,5-di-t-butylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

98%

Reagent Code: #68653
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CAS Number 1365531-98-1

science Other reagents with same CAS 1365531-98-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1211.61 g/mol
Formula C₇₆H₁₀₈O₈P₂
badge Registry Numbers
MDL Number MFCD22666441
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring bulky substituents and methoxy groups, enhances steric and electronic control, making it highly effective in enantioselective transformations. It is commonly employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where high enantiomeric excess is crucial. Its application is particularly significant in the pharmaceutical industry for synthesizing chiral intermediates and active pharmaceutical ingredients (APIs) with precise stereochemistry. Additionally, it finds use in academic research to develop novel catalytic methodologies and study asymmetric induction mechanisms.

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Test Parameter Specification
Appearance White to Faint Yellow and Faint Beige and Faint Brown Powder or Crystals
Purity (%) 97.5-100
Specific Rotation ([alpha]20/D (C=0.5,CHCl3))(degree) 13-23
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,800.00
inventory 250mg
10-20 days ฿34,800.00

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(R)-2,2'-Bis[bis(4-methoxy-3,5-di-t-butylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring bulky substituents and methoxy groups, enhances steric and electronic control, making it highly effective in enantioselective transformations. It is commonly employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where high enantiomeric excess is crucial. Its application is particularly significant in the phar

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring bulky substituents and methoxy groups, enhances steric and electronic control, making it highly effective in enantioselective transformations. It is commonly employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where high enantiomeric excess is crucial. Its application is particularly significant in the pharmaceutical industry for synthesizing chiral intermediates and active pharmaceutical ingredients (APIs) with precise stereochemistry. Additionally, it finds use in academic research to develop novel catalytic methodologies and study asymmetric induction mechanisms.

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