(S)-4-Phenyl-2-(2-(pyridin-2-yl)propan-2-yl)-4,5-dihydrooxazole

97%

Reagent Code: #237868
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CAS Number 292839-81-7

science Other reagents with same CAS 292839-81-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.34 g/mol
Formula C₁₇H₁₈N₂O
badge Registry Numbers
MDL Number MFCD34563687
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. Its oxazoline core combined with pyridine and phenyl groups allows it to form stable complexes with transition metals, making it effective in enantioselective hydrogenation and C–C bond-forming reactions. Commonly applied in pharmaceutical synthesis to produce enantiomerically pure compounds, especially in the development of active pharmaceutical ingredients (APIs) where stereochemistry is critical. Its rigid structure enhances stereocontrol, improving yield and selectivity in complex organic transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,380.00
(S)-4-Phenyl-2-(2-(pyridin-2-yl)propan-2-yl)-4,5-dihydrooxazole
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Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. Its oxazoline core combined with pyridine and phenyl groups allows it to form stable complexes with transition metals, making it effective in enantioselective hydrogenation and C–C bond-forming reactions. Commonly applied in pharmaceutical synthesis to produce enantiomerically pure compounds, especially in the development of active pharmaceutical ingredients (API

Used as a chiral ligand or intermediate in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. Its oxazoline core combined with pyridine and phenyl groups allows it to form stable complexes with transition metals, making it effective in enantioselective hydrogenation and C–C bond-forming reactions. Commonly applied in pharmaceutical synthesis to produce enantiomerically pure compounds, especially in the development of active pharmaceutical ingredients (APIs) where stereochemistry is critical. Its rigid structure enhances stereocontrol, improving yield and selectivity in complex organic transformations.

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