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

97%

Reagent Code: #236576
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CAS Number 404844-76-4

science Other reagents with same CAS 404844-76-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.28 g/mol
Formula C₁₅H₁₄N₂O
badge Registry Numbers
MDL Number MFCD34563691
thermostat Physical Properties
Boiling Point 386.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage Room temperature, 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 a pyridine substituent enables 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,540.00
inventory 250mg
10-20 days ฿6,050.00
inventory 1g
10-20 days ฿22,770.00
(S)-4-Phenyl-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 a pyridine substituent enables 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 l

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective carbon-carbon bond-forming reactions. Its oxazoline core with a pyridine substituent enables 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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