(3aS,3a'S,3a"S,8aR,8a'R,8a"R)-2,2',2"-(Propane-1,2,2-triyl)tris(8,8a-dihydro-3aH-indeno[1,2-d]oxazole)

95%

Reagent Code: #55494
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CAS Number 1239015-11-2

science Other reagents with same CAS 1239015-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 515.6017 g/mol
Formula C₃₃H₂₉N₃O₃
badge Registry Numbers
MDL Number MFCD27978385
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chiral tris(indenooxazoline) ligand is employed in asymmetric catalysis, facilitating enantioselective transformations in organic synthesis. Its rigid, C3-symmetric structure enables high stereocontrol in metal-catalyzed reactions, such as allylic alkylations and cyclizations, making it valuable for producing enantiomerically pure intermediates in pharmaceutical and agrochemical industries. Additionally, it serves as a research tool in coordination chemistry to explore mechanistic aspects of catalytic processes.

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inventory 100mg
10-20 days ฿5,400.00

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(3aS,3a'S,3a"S,8aR,8a'R,8a"R)-2,2',2"-(Propane-1,2,2-triyl)tris(8,8a-dihydro-3aH-indeno[1,2-d]oxazole)
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This chiral tris(indenooxazoline) ligand is employed in asymmetric catalysis, facilitating enantioselective transformations in organic synthesis. Its rigid, C3-symmetric structure enables high stereocontrol in metal-catalyzed reactions, such as allylic alkylations and cyclizations, making it valuable for producing enantiomerically pure intermediates in pharmaceutical and agrochemical industries. Additionally, it serves as a research tool in coordination chemistry to explore mechanistic aspects of catalyt

This chiral tris(indenooxazoline) ligand is employed in asymmetric catalysis, facilitating enantioselective transformations in organic synthesis. Its rigid, C3-symmetric structure enables high stereocontrol in metal-catalyzed reactions, such as allylic alkylations and cyclizations, making it valuable for producing enantiomerically pure intermediates in pharmaceutical and agrochemical industries. Additionally, it serves as a research tool in coordination chemistry to explore mechanistic aspects of catalytic processes.

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