(3aR,3a'R,8aS,8a'S)-2,2'-(Cyclobutane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole)

97%,99%ee

Reagent Code: #36714
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CAS Number 2097145-90-7

science Other reagents with same CAS 2097145-90-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 370.4400 g/mol
Formula C₂₄H₂₂N₂O₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is a chiral bis(oxazoline) ligand with a cyclobutane-1,1-diyl linker connecting two indeno[1,2-d]oxazole units, featuring specific (3aR,3a'R,8aS,8a'S) stereochemistry. It is primarily utilized as a ligand in asymmetric catalysis, forming complexes with transition metals such as copper, palladium, or ruthenium to enable enantioselective transformations. Key applications include enantioselective cyclopropanation, allylic substitution, Diels-Alder reactions, and other C-C or C-N bond-forming processes, which are essential for synthesizing enantiomerically pure pharmaceuticals, agrochemicals, and advanced materials. Its rigid, bidentate structure provides excellent control over stereoselectivity, often achieving high enantiomeric excess (ee) values.

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Test Parameter Specification
Appearance Off-White to Light Yellow Solid
Purity (%) 96.5-100%
EE % 99-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,068.00

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(3aR,3a'R,8aS,8a'S)-2,2'-(Cyclobutane-1,1-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole)
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This compound is a chiral bis(oxazoline) ligand with a cyclobutane-1,1-diyl linker connecting two indeno[1,2-d]oxazole units, featuring specific (3aR,3a'R,8aS,8a'S) stereochemistry. It is primarily utilized as a ligand in asymmetric catalysis, forming complexes with transition metals such as copper, palladium, or ruthenium to enable enantioselective transformations. Key applications include enantioselective cyclopropanation, allylic substitution, Diels-Alder reactions, and other C-C or C-N bond-forming p

This compound is a chiral bis(oxazoline) ligand with a cyclobutane-1,1-diyl linker connecting two indeno[1,2-d]oxazole units, featuring specific (3aR,3a'R,8aS,8a'S) stereochemistry. It is primarily utilized as a ligand in asymmetric catalysis, forming complexes with transition metals such as copper, palladium, or ruthenium to enable enantioselective transformations. Key applications include enantioselective cyclopropanation, allylic substitution, Diels-Alder reactions, and other C-C or C-N bond-forming processes, which are essential for synthesizing enantiomerically pure pharmaceuticals, agrochemicals, and advanced materials. Its rigid, bidentate structure provides excellent control over stereoselectivity, often achieving high enantiomeric excess (ee) values.

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