(S)-4-((S)-sec-Butyl)-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole

95%

Reagent Code: #237443
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CAS Number 2828439-59-2

science Other reagents with same CAS 2828439-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.27 g/mol
Formula C₁₃H₁₅F₃N₂O
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Its oxazole core and trifluoromethylpyridine moiety contribute to enhanced metabolic stability and binding selectivity. Commonly employed in asymmetric synthesis to construct complex molecules where stereochemistry is critical for activity. Also utilized in agrochemical research for creating enantiomerically pure herbicides and pesticides with improved environmental profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,740.00
inventory 250mg
10-20 days ฿20,960.00
inventory 1g
10-20 days ฿70,650.00
(S)-4-((S)-sec-Butyl)-2-(5-(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 the development of pharmaceuticals targeting central nervous system disorders. Its oxazole core and trifluoromethylpyridine moiety contribute to enhanced metabolic stability and binding selectivity. Commonly employed in asymmetric synthesis to construct complex molecules where stereochemistry is critical for activity. Also utilized in agrochemical research for creating enantiomerically pure herbicides and pes

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Its oxazole core and trifluoromethylpyridine moiety contribute to enhanced metabolic stability and binding selectivity. Commonly employed in asymmetric synthesis to construct complex molecules where stereochemistry is critical for activity. Also utilized in agrochemical research for creating enantiomerically pure herbicides and pesticides with improved environmental profiles.

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