(R)-4-(tert-Butyl)-2-(quinolin-2-yl)-4,5-dihydrooxazole

97%, 99% e.e.

Reagent Code: #229302
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CAS Number 2634687-57-1

science Other reagents with same CAS 2634687-57-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.32 g/mol
Formula C₁₆H₁₈N₂O
thermostat Physical Properties
Boiling Point 399.4±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.13±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral auxiliary or catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its rigid oxazoline-quinoline framework enables strong coordination to metal centers, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The compound is valued for its ability to induce high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. It is also employed in the development of novel ligands for transition-metal-catalyzed transformations, where stereocontrol is critical.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,390.00
1g
10-20 days ฿10,000.00
250mg
10-20 days ฿3,390.00
(R)-4-(tert-Butyl)-2-(quinolin-2-yl)-4,5-dihydrooxazole
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Used as a chiral auxiliary or catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its rigid oxazoline-quinoline framework enables strong coordination to metal centers, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The compound is valued for its ability to induce high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. It is also employed in the developme

Used as a chiral auxiliary or catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its rigid oxazoline-quinoline framework enables strong coordination to metal centers, making it effective in catalyzing reactions such as asymmetric allylic alkylation and Diels-Alder reactions. The compound is valued for its ability to induce high enantiomeric excess in the synthesis of pharmaceutical intermediates and fine chemicals. It is also employed in the development of novel ligands for transition-metal-catalyzed transformations, where stereocontrol is critical.

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