(3AR,3a'R,8aS,8a'S)-2,2'-(1-phenylpropane-2,2-diyl)bis(8,8a-dihydro-3aH-indeno[1,2-d]oxazole)

97%, 99%e.e.

Reagent Code: #138995
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CAS Number 2757082-37-2

science Other reagents with same CAS 2757082-37-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 434.52 g/mol
Formula C₂₉H₂₆N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid bisoxazole framework provides excellent stereocontrol in metal-catalyzed reactions such as hydrogenations, C–C bond formations, and cycloadditions. The compound is effective in coordinating transition metals like rhodium, ruthenium, and palladium, enabling high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Due to its C2-symmetric structure, it promotes uniform spatial orientation of substrates during catalytic cycles, enhancing reaction precision. Commonly employed in research settings for developing enantiopure compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,510.00
inventory 250mg
10-20 days ฿19,910.00
inventory 1g
10-20 days ฿57,540.00

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(3AR,3a'R,8aS,8a'S)-2,2'-(1-phenylpropane-2,2-diyl)bis(8,8a-dihydro-3aH-indeno[1,2-d]oxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid bisoxazole framework provides excellent stereocontrol in metal-catalyzed reactions such as hydrogenations, C–C bond formations, and cycloadditions. The compound is effective in coordinating transition metals like rhodium, ruthenium, and palladium, enabling high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Due to its C2-symmetric structure, it promotes uniform

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid bisoxazole framework provides excellent stereocontrol in metal-catalyzed reactions such as hydrogenations, C–C bond formations, and cycloadditions. The compound is effective in coordinating transition metals like rhodium, ruthenium, and palladium, enabling high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Due to its C2-symmetric structure, it promotes uniform spatial orientation of substrates during catalytic cycles, enhancing reaction precision. Commonly employed in research settings for developing enantiopure compounds.

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