2,6-Bis[(2R,4S,5S)-1-benzyl-4,5-diphenylimidazolidin-2-yl]pyridine

90%

Reagent Code: #69832
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CAS Number 1223020-29-8

science Other reagents with same CAS 1223020-29-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 703.9299999999999 g/mol
Formula C₄₉H₄₅N₅
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its structure, featuring imidazolidine rings and a central pyridine core, allows it to effectively coordinate with metal centers, enhancing stereoselectivity in various reactions. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where precise control over chiral induction is critical. Its application is valuable in the pharmaceutical industry for producing chiral drugs and intermediates with high enantiomeric purity. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring stereochemical outcomes in organic synthesis.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 89.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿1,880.00
inventory 50mg
10-20 days ฿5,310.00

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2,6-Bis[(2R,4S,5S)-1-benzyl-4,5-diphenylimidazolidin-2-yl]pyridine
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its structure, featuring imidazolidine rings and a central pyridine core, allows it to effectively coordinate with metal centers, enhancing stereoselectivity in various reactions. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where precise control over chiral induction is critical. Its applicatio

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in the synthesis of enantiomerically pure compounds. Its structure, featuring imidazolidine rings and a central pyridine core, allows it to effectively coordinate with metal centers, enhancing stereoselectivity in various reactions. It is often employed in enantioselective hydrogenation, carbon-carbon bond formation, and other transformations where precise control over chiral induction is critical. Its application is valuable in the pharmaceutical industry for producing chiral drugs and intermediates with high enantiomeric purity. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring stereochemical outcomes in organic synthesis.

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