(3aS,​3'aS,​8aR,​8'aR)​-2,​2'-​Cyclopentylidenebis[​3a,​8a-​dihydro-8H-indeno[1,​2-​d]​oxazole]

≥98%,99%e.e.

Reagent Code: #59692
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CAS Number 182122-12-9

science Other reagents with same CAS 182122-12-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.5 g/mol
Formula C₂₅H₂₄N₂O₂
thermostat Physical Properties
Boiling Point 539.7±50.0 °C
inventory_2 Storage & Handling
Density 1.46±0.1 g/mL
Storage room temperature, dry

description Product Description

This chiral bis(oxazoline) compound, featuring a rigid indeno[1,2-d]oxazole framework bridged by a cyclopentylidene group, is primarily utilized as a ligand in asymmetric catalysis. Its specific (3aS,3'aS,8aR,8'aR) stereochemistry enables high enantioselectivity in metal-catalyzed reactions, such as copper-mediated enantioselective cyclopropanations, allylic oxidations, and Diels-Alder reactions. This makes it invaluable for the synthesis of enantiomerically pure intermediates in pharmaceutical production, including drugs targeting chiral molecular targets. Unlike general intermediates, it functions as a reusable catalyst component rather than a stoichiometric reagent, highlighting its role as a specialty chemical in advanced organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,628.00

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(3aS,​3'aS,​8aR,​8'aR)​-2,​2'-​Cyclopentylidenebis[​3a,​8a-​dihydro-8H-indeno[1,​2-​d]​oxazole]
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This chiral bis(oxazoline) compound, featuring a rigid indeno[1,2-d]oxazole framework bridged by a cyclopentylidene group, is primarily utilized as a ligand in asymmetric catalysis. Its specific (3aS,3'aS,8aR,8'aR) stereochemistry enables high enantioselectivity in metal-catalyzed reactions, such as copper-mediated enantioselective cyclopropanations, allylic oxidations, and Diels-Alder reactions. This makes it invaluable for the synthesis of enantiomerically pure intermediates in pharmaceutical productio

This chiral bis(oxazoline) compound, featuring a rigid indeno[1,2-d]oxazole framework bridged by a cyclopentylidene group, is primarily utilized as a ligand in asymmetric catalysis. Its specific (3aS,3'aS,8aR,8'aR) stereochemistry enables high enantioselectivity in metal-catalyzed reactions, such as copper-mediated enantioselective cyclopropanations, allylic oxidations, and Diels-Alder reactions. This makes it invaluable for the synthesis of enantiomerically pure intermediates in pharmaceutical production, including drugs targeting chiral molecular targets. Unlike general intermediates, it functions as a reusable catalyst component rather than a stoichiometric reagent, highlighting its role as a specialty chemical in advanced organic synthesis.

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