1,3-Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)benzene

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Reagent Code: #153629
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CAS Number 876953-19-4

science Other reagents with same CAS 876953-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.43 g/mol
Formula C₂₄H₂₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective organic transformations. It forms stable complexes with transition metals such as rhodium, ruthenium, and iridium, which are employed in hydrogenation reactions of prochiral substrates like ketones, alkenes, and imines. Due to its rigid aromatic backbone and well-defined chiral environment, it helps achieve high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. Its effectiveness in asymmetric synthesis makes it valuable in academic research and industrial drug development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,000.00
inventory 250mg
10-20 days ฿4,760.00
inventory 1g
10-20 days ฿11,890.00

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1,3-Bis((S)-4-phenyl-4,5-dihydrooxazol-2-yl)benzene
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective organic transformations. It forms stable complexes with transition metals such as rhodium, ruthenium, and iridium, which are employed in hydrogenation reactions of prochiral substrates like ketones, alkenes, and imines. Due to its rigid aromatic backbone and well-defined chiral environment, it helps achieve high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals.

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective organic transformations. It forms stable complexes with transition metals such as rhodium, ruthenium, and iridium, which are employed in hydrogenation reactions of prochiral substrates like ketones, alkenes, and imines. Due to its rigid aromatic backbone and well-defined chiral environment, it helps achieve high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. Its effectiveness in asymmetric synthesis makes it valuable in academic research and industrial drug development.

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