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

97%

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

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.2396 g/mol
Formula C₁₂H₁₃F₃N₂O
inventory_2 Storage & Handling
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description Product Description

(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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿2,232.00
(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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