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

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Reagent Code: #237484
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CAS Number 2757085-31-5

science Other reagents with same CAS 2757085-31-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.22 g/mol
Formula C₁₀H₁₂N₂O
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective hydrogenation and C–C 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 employed in research settings for designing catalysts with improved selectivity and reactivity under mild reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,390.00
inventory 250mg
10-20 days ฿18,420.00
inventory 1g
10-20 days ฿48,450.00

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(S)-4-Methyl-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 C–C 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 employed i

Used as a chiral catalyst or ligand in asymmetric synthesis, particularly in enantioselective hydrogenation and C–C 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 employed in research settings for designing catalysts with improved selectivity and reactivity under mild reaction conditions.

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