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

97%, 99% e.e.

Reagent Code: #229424
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CAS Number 2635322-22-2

science Other reagents with same CAS 2635322-22-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.35 g/mol
Formula C₂₁H₁₅F₃N₂O
thermostat Physical Properties
Boiling Point 473.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.28±0.1 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of pharmaceuticals. Its rigid oxazoline core and stereocenters enable high enantioselectivity in catalytic reactions, such as cycloadditions or metal-mediated couplings. The trifluoromethylpyridine group enhances binding affinity in biologically active molecules, making this compound valuable in medicinal chemistry for designing enzyme inhibitors or receptor modulators. It is also employed in the synthesis of complex natural products where stereocontrol is critical.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,020.00
250mg
10-20 days ฿8,060.00
(4R,5S)-4,5-Diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of pharmaceuticals. Its rigid oxazoline core and stereocenters enable high enantioselectivity in catalytic reactions, such as cycloadditions or metal-mediated couplings. The trifluoromethylpyridine group enhances binding affinity in biologically active molecules, making this compound valuable in medicinal chemistry for designing enzyme inhibitors or receptor modulators. It is also employed in the synthesis

Used as a chiral auxiliary or intermediate in asymmetric synthesis, particularly in the development of pharmaceuticals. Its rigid oxazoline core and stereocenters enable high enantioselectivity in catalytic reactions, such as cycloadditions or metal-mediated couplings. The trifluoromethylpyridine group enhances binding affinity in biologically active molecules, making this compound valuable in medicinal chemistry for designing enzyme inhibitors or receptor modulators. It is also employed in the synthesis of complex natural products where stereocontrol is critical.

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