(S)-4-Benzyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole

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Reagent Code: #236960
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CAS Number 404844-73-1

science Other reagents with same CAS 404844-73-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.31 g/mol
Formula C₁₆H₁₆N₂O
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective hydrogenation and carbon-carbon bond-forming reactions. Its oxazoline-pyridine framework coordinates well with transition metals like palladium, nickel, and iridium, enhancing stereochemical control in the production of pharmaceutical intermediates and fine chemicals. Commonly applied in the development of optically active compounds for drug synthesis, especially where high enantiomeric excess is required. Also utilized in research settings for designing catalysts with improved selectivity and activity under mild reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,910.00

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(S)-4-Benzyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole
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Used as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective hydrogenation and carbon-carbon bond-forming reactions. Its oxazoline-pyridine framework coordinates well with transition metals like palladium, nickel, and iridium, enhancing stereochemical control in the production of pharmaceutical intermediates and fine chemicals. Commonly applied in the development of optically active compounds for drug synthesis, especially where high enantiomeric excess is required. Also

Used as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective hydrogenation and carbon-carbon bond-forming reactions. Its oxazoline-pyridine framework coordinates well with transition metals like palladium, nickel, and iridium, enhancing stereochemical control in the production of pharmaceutical intermediates and fine chemicals. Commonly applied in the development of optically active compounds for drug synthesis, especially where high enantiomeric excess is required. Also utilized in research settings for designing catalysts with improved selectivity and activity under mild reaction conditions.

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