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

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Reagent Code: #38512
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CAS Number 1416820-34-2

science Other reagents with same CAS 1416820-34-2

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Weight 258.2396 g/mol
Formula C₁₂H₁₃F₃N₂O
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(S)-4-Isopropyl-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is a chiral pyridine-oxazoline (PyOx) ligand extensively used in asymmetric catalysis for the synthesis of enantiomerically pure compounds. It excels in metal-catalyzed reactions such as enantioselective allylic alkylations, conjugate additions, and C-H functionalizations, particularly with copper, palladium, or iridium catalysts. The electron-withdrawing trifluoromethyl group on the pyridine ring tunes the ligand's electronics for enhanced reactivity and selectivity, while the (S)-isopropyl-substituted oxazoline provides crucial steric control. This makes it invaluable in medicinal chemistry for preparing chiral building blocks and intermediates for pharmaceuticals targeting neurological disorders, cancers, and other diseases.

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inventory 50mg
10-20 days ฿2,232.00

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(S)-4-Isopropyl-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
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(S)-4-Isopropyl-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is a chiral pyridine-oxazoline (PyOx) ligand extensively used in asymmetric catalysis for the synthesis of enantiomerically pure compounds. It excels in metal-catalyzed reactions such as enantioselective allylic alkylations, conjugate additions, and C-H functionalizations, particularly with copper, palladium, or iridium catalysts. The electron-withdrawing trifluoromethyl group on the pyridine ring tunes the ligand's electronics for en

(S)-4-Isopropyl-2-(4-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole is a chiral pyridine-oxazoline (PyOx) ligand extensively used in asymmetric catalysis for the synthesis of enantiomerically pure compounds. It excels in metal-catalyzed reactions such as enantioselective allylic alkylations, conjugate additions, and C-H functionalizations, particularly with copper, palladium, or iridium catalysts. The electron-withdrawing trifluoromethyl group on the pyridine ring tunes the ligand's electronics for enhanced reactivity and selectivity, while the (S)-isopropyl-substituted oxazoline provides crucial steric control. This makes it invaluable in medicinal chemistry for preparing chiral building blocks and intermediates for pharmaceuticals targeting neurological disorders, cancers, and other diseases.

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