rel-2,6-Bis((S)-4-isopropyl-4,5-dihydrooxazol-2-yl)pyridine

≥98%

Reagent Code: #156044
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CAS Number 173829-03-3

science Other reagents with same CAS 173829-03-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.38 g/mol
Formula C₁₇H₂₃N₃O₂
thermostat Physical Properties
Melting Point 155-157 °C(lit.)
Boiling Point 457.1±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation, cyclopropanation, and Diels-Alder reactions. Its rigid pyridine backbone and oxazoline rings provide excellent stereocontrol when coordinated to transition metals like copper, nickel, or iridium. It is particularly effective in promoting high enantioselectivity in C–C bond-forming reactions and in the synthesis of optically active pharmaceutical intermediates. Due to its modular synthesis and tunable steric environment, it is favored in both academic research and industrial processes for producing single-enantiomer compounds.

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inventory 1g
10-20 days ฿2,040.00

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rel-2,6-Bis((S)-4-isopropyl-4,5-dihydrooxazol-2-yl)pyridine
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation, cyclopropanation, and Diels-Alder reactions. Its rigid pyridine backbone and oxazoline rings provide excellent stereocontrol when coordinated to transition metals like copper, nickel, or iridium. It is particularly effective in promoting high enantioselectivity in C–C bond-forming reactions and in the synthesis of optically active pharmaceutical intermediates.

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation, cyclopropanation, and Diels-Alder reactions. Its rigid pyridine backbone and oxazoline rings provide excellent stereocontrol when coordinated to transition metals like copper, nickel, or iridium. It is particularly effective in promoting high enantioselectivity in C–C bond-forming reactions and in the synthesis of optically active pharmaceutical intermediates. Due to its modular synthesis and tunable steric environment, it is favored in both academic research and industrial processes for producing single-enantiomer compounds.

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