(4S, 4'S)-2, 2'-(4-Bromopyridine-2, 6-diyl)bis(4-isopropyl-4, 5-dihydrooxazole)

98%

Reagent Code: #236518
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CAS Number 477351-96-5

science Other reagents with same CAS 477351-96-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 380.28 g/mol
Formula C₁₇H₂₂BrN₃O₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as cyclopropanation, aldol, and allylic alkylation reactions. Its rigid pyridine backbone and chiral oxazoline rings enhance stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly coordinates with transition metals like copper or palladium to form highly selective catalysts. Preferred in reactions requiring high enantiomeric excess and reproducibility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,200.00
inventory 1g
10-20 days ฿30,260.00
inventory 250mg
10-20 days ฿8,550.00
(4S, 4'S)-2, 2'-(4-Bromopyridine-2, 6-diyl)bis(4-isopropyl-4, 5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as cyclopropanation, aldol, and allylic alkylation reactions. Its rigid pyridine backbone and chiral oxazoline rings enhance stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly coordinates with transition metals like copper or palladium to form highly selective catalysts. Preferred in reactions requiring high enantiomeric excess and

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as cyclopropanation, aldol, and allylic alkylation reactions. Its rigid pyridine backbone and chiral oxazoline rings enhance stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly coordinates with transition metals like copper or palladium to form highly selective catalysts. Preferred in reactions requiring high enantiomeric excess and reproducibility.

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