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

≥98%,99%e.e.

Reagent Code: #59694
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CAS Number 175166-51-5

science Other reagents with same CAS 175166-51-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.4 g/mol
Formula C₂₃H₂₂N₂O₂
thermostat Physical Properties
Melting Point 177-178°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is a highly specific chiral bis(oxazoline) ligand with a rigid, fused indeno[1,2-d]oxazole framework and defined (3aS,3'aS,8aR,8'aR) stereochemistry. It is primarily employed as a key ligand in the development and application of chiral catalysts for asymmetric synthesis, particularly in pharmaceutical manufacturing where high enantioselectivity (≥99% e.e.) is required for producing enantiomerically pure drugs. Its unique structure enables stereocontrol in reactions such as enantioselective hydrogenations, allylations, and other C-C bond formations. Available at ≥98% purity, it is a niche specialty chemical for advanced organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,095.00
inventory 100mg
10-20 days ฿2,259.00
inventory 250mg
10-20 days ฿3,852.00

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(3aS,3'aS,8aR,8'aR)-2,2'-(1-Methylethylidene)bis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole]
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This compound is a highly specific chiral bis(oxazoline) ligand with a rigid, fused indeno[1,2-d]oxazole framework and defined (3aS,3'aS,8aR,8'aR) stereochemistry. It is primarily employed as a key ligand in the development and application of chiral catalysts for asymmetric synthesis, particularly in pharmaceutical manufacturing where high enantioselectivity (≥99% e.e.) is required for producing enantiomerically pure drugs. Its unique structure enables stereocontrol in reactions such as enantioselective

This compound is a highly specific chiral bis(oxazoline) ligand with a rigid, fused indeno[1,2-d]oxazole framework and defined (3aS,3'aS,8aR,8'aR) stereochemistry. It is primarily employed as a key ligand in the development and application of chiral catalysts for asymmetric synthesis, particularly in pharmaceutical manufacturing where high enantioselectivity (≥99% e.e.) is required for producing enantiomerically pure drugs. Its unique structure enables stereocontrol in reactions such as enantioselective hydrogenations, allylations, and other C-C bond formations. Available at ≥98% purity, it is a niche specialty chemical for advanced organic synthesis.

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