(S)-2-(Benzo[h]quinolin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole

98%

Reagent Code: #236933
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CAS Number 284483-04-1

science Other reagents with same CAS 284483-04-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.39 g/mol
Formula C₂₀H₂₀N₂O
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H activation and cyclization reactions. Its rigid oxazole framework and extended aromatic system enhance stereocontrol, making it effective in promoting high enantioselectivity in the formation of chiral heterocycles and functionalized hydrocarbons. Commonly applied in pharmaceutical synthesis where precise stereochemistry is critical. Also utilized in coordination chemistry as a ligand for transition metals such as palladium and rhodium to facilitate asymmetric catalysis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,180.00
inventory 250mg
10-20 days ฿20,090.00
inventory 1g
10-20 days ฿56,090.00
(S)-2-(Benzo[h]quinolin-2-yl)-4-(tert-butyl)-4,5-dihydrooxazole
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Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H activation and cyclization reactions. Its rigid oxazole framework and extended aromatic system enhance stereocontrol, making it effective in promoting high enantioselectivity in the formation of chiral heterocycles and functionalized hydrocarbons. Commonly applied in pharmaceutical synthesis where precise stereochemistry is critical. Also utilized in coordination chemistry as a ligand for transition metals such as pal

Used as a chiral catalyst in asymmetric synthesis, particularly in enantioselective C–H activation and cyclization reactions. Its rigid oxazole framework and extended aromatic system enhance stereocontrol, making it effective in promoting high enantioselectivity in the formation of chiral heterocycles and functionalized hydrocarbons. Commonly applied in pharmaceutical synthesis where precise stereochemistry is critical. Also utilized in coordination chemistry as a ligand for transition metals such as palladium and rhodium to facilitate asymmetric catalysis.

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