(S)-4-Benzyl-2-(quinolin-8-yl)-4,5-dihydrooxazole

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Reagent Code: #236831
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CAS Number 220628-97-7

science Other reagents with same CAS 220628-97-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.34 g/mol
Formula C₁₉H₁₆N₂O
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. It is effective in promoting reactions such as aldol additions and allylic alkylations, where high enantiomeric excess is required. Its structure allows for strong coordination with metal ions like copper or nickel, enhancing stereocontrol in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly applied in research settings for developing optically active compounds, including bioactive molecules and natural product analogs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,140.00
inventory 250mg
10-20 days ฿19,930.00
inventory 1g
10-20 days ฿57,550.00

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(S)-4-Benzyl-2-(quinolin-8-yl)-4,5-dihydrooxazole
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Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. It is effective in promoting reactions such as aldol additions and allylic alkylations, where high enantiomeric excess is required. Its structure allows for strong coordination with metal ions like copper or nickel, enhancing stereocontrol in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly applied in research settings for developing optically active compound

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. It is effective in promoting reactions such as aldol additions and allylic alkylations, where high enantiomeric excess is required. Its structure allows for strong coordination with metal ions like copper or nickel, enhancing stereocontrol in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly applied in research settings for developing optically active compounds, including bioactive molecules and natural product analogs.

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