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

97%, 99% e.e.

Reagent Code: #229478
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CAS Number 2828432-07-9

science Other reagents with same CAS 2828432-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.26 g/mol
Formula C₁₃H₁₅F₃N₂O
thermostat Physical Properties
Boiling Point 335.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazole core and trifluoromethylpyridine moiety enhance binding selectivity and metabolic stability. Commonly employed in asymmetric synthesis to introduce stereochemical control in drug candidates. Also utilized in agrochemicals for developing enantioselective herbicides and pesticides due to its structural rigidity and resistance to degradation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,970.00
inventory 250mg
10-20 days ฿12,340.00
inventory 1g
10-20 days ฿35,650.00

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(R)-4-(tert-Butyl)-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazole core and trifluoromethylpyridine moiety enhance binding selectivity and metabolic stability. Commonly employed in asymmetric synthesis to introduce stereochemical control in drug candidates. Also utilized in agrochemicals for developing enantioselective herbicides and pesticides due to its structural rigidity and resistance to degradation

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its oxazole core and trifluoromethylpyridine moiety enhance binding selectivity and metabolic stability. Commonly employed in asymmetric synthesis to introduce stereochemical control in drug candidates. Also utilized in agrochemicals for developing enantioselective herbicides and pesticides due to its structural rigidity and resistance to degradation.

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