(S)-2,2'-Bis[bis(3,5-dimethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

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Reagent Code: #37997
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CAS Number 1365531-90-3

science Other reagents with same CAS 1365531-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 754.8700 g/mol
Formula C₄₈H₅₂O₄P₂
badge Registry Numbers
MDL Number MFCD19443624
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its highly sterically hindered and electron-rich structure makes it effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. The ligand's ability to induce high enantiomeric excess in the formation of chiral compounds is valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its application is especially prominent in the production of optically active intermediates, contributing to the development of drugs with specific stereochemical requirements.

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inventory 50mg
10-20 days ฿3,609.00

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(S)-2,2'-Bis[bis(3,5-dimethylphenyl)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 highly sterically hindered and electron-rich structure makes it effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. The ligand's ability to induce high enantiomeric excess in the formation of chiral compounds is valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemic

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its highly sterically hindered and electron-rich structure makes it effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. The ligand's ability to induce high enantiomeric excess in the formation of chiral compounds is valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its application is especially prominent in the production of optically active intermediates, contributing to the development of drugs with specific stereochemical requirements.

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