(4R,5S)-4,5-Diphenyl-2-(pyridin-2-ylmethyl)-4,5-dihydrooxazole

97%

Reagent Code: #231849
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CAS Number 2757085-37-1

science Other reagents with same CAS 2757085-37-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.38 g/mol
Formula C₂₁H₁₈N₂O
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline core with defined stereochemistry enables high stereoselectivity in transformations such as aldol reactions, Diels-Alder cycloadditions, and allylations. Commonly employed in pharmaceutical research for constructing optically active intermediates. Also utilized in coordination chemistry as a ligand for transition metals like copper or palladium to form catalytically active complexes. Shows good stability under various reaction conditions, making it suitable for both academic and industrial applications in fine chemical synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,220.00
inventory 250mg
10-20 days ฿19,060.00
inventory 1g
10-20 days ฿55,060.00
(4R,5S)-4,5-Diphenyl-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 with defined stereochemistry enables high stereoselectivity in transformations such as aldol reactions, Diels-Alder cycloadditions, and allylations. Commonly employed in pharmaceutical research for constructing optically active intermediates. Also utilized in coordination chemistry as a ligand for transition metals like copper or palladium to form catalytically acti

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline core with defined stereochemistry enables high stereoselectivity in transformations such as aldol reactions, Diels-Alder cycloadditions, and allylations. Commonly employed in pharmaceutical research for constructing optically active intermediates. Also utilized in coordination chemistry as a ligand for transition metals like copper or palladium to form catalytically active complexes. Shows good stability under various reaction conditions, making it suitable for both academic and industrial applications in fine chemical synthesis.

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