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

97%

Reagent Code: #236825
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CAS Number 217653-18-4

science Other reagents with same CAS 217653-18-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.26 g/mol
Formula C₁₂H₁₆N₂O
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. Its oxazoline core and pyridine moiety enable strong coordination with transition metals, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The (S)-configuration ensures high enantioselectivity, which is crucial for producing optically active intermediates in pharmaceuticals and fine chemicals. Commonly employed in research and industrial settings for the synthesis of complex molecules requiring precise stereochemical control.

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inventory 100mg
10-20 days ฿3,960.00

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(S)-4-Isopropyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole
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Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline core and pyridine moiety enable strong coordination with transition metals, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The (S)-configuration ensures high enantioselectivity, which is crucial for producing optically active intermediates in pharmaceuticals and fine chemicals. Commonly employed in research an

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline core and pyridine moiety enable strong coordination with transition metals, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The (S)-configuration ensures high enantioselectivity, which is crucial for producing optically active intermediates in pharmaceuticals and fine chemicals. Commonly employed in research and industrial settings for the synthesis of complex molecules requiring precise stereochemical control.

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