2,2'-(Propane-2,2-diyl)bis(4,5-dihydrooxazole)

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Reagent Code: #228313
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CAS Number 165554-94-9

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Weight 182.22 g/mol
Formula C₉H₁₄N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It coordinates with transition metals to form catalysts that promote stereoselective reactions such as aldol condensations, Diels-Alder reactions, and alkylations. Its rigid structure and ability to form stable complexes enhance enantioselectivity and reaction efficiency. Commonly employed in pharmaceutical synthesis where precise stereochemistry is critical. Also utilized in polymer chemistry as a modifier to influence polymer tacticity and in the development of chiral stationary phases for chromatographic separation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,660.00
inventory 250mg
10-20 days ฿9,400.00
inventory 1g
10-20 days ฿28,700.00

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2,2'-(Propane-2,2-diyl)bis(4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It coordinates with transition metals to form catalysts that promote stereoselective reactions such as aldol condensations, Diels-Alder reactions, and alkylations. Its rigid structure and ability to form stable complexes enhance enantioselectivity and reaction efficiency. Commonly employed in pharmaceutical synthesis where precise stereochemistry is critical. Also utilized in polymer chemistry as a

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It coordinates with transition metals to form catalysts that promote stereoselective reactions such as aldol condensations, Diels-Alder reactions, and alkylations. Its rigid structure and ability to form stable complexes enhance enantioselectivity and reaction efficiency. Commonly employed in pharmaceutical synthesis where precise stereochemistry is critical. Also utilized in polymer chemistry as a modifier to influence polymer tacticity and in the development of chiral stationary phases for chromatographic separation.

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