[3aR-[2(3'aR*,8'aS*),3'aβ,8'aβ]]-()-2,2'-Methylenebis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole]

98%

Reagent Code: #126739
label
Alias (+)-2,2'-Methylenebis[(3aR,8aS)-3a,8a-dihydro-8H-indenebenzo[1,2-d]oxazole
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CAS Number 180186-94-1

science Other reagents with same CAS 180186-94-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.38 g/mol
Formula C₂₁H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD00674092
thermostat Physical Properties
Melting Point 225 °C
inventory_2 Storage & Handling
Density 1.48
Storage room temperature

description Product Description

This chiral bis(oxazoline) ligand, featuring a rigid indeno-fused structure connected by a methylene bridge, is primarily utilized in asymmetric catalysis. It coordinates with transition metals such as copper, palladium, or ruthenium to enable highly enantioselective reactions, including Diels-Alder cycloadditions, aldol reactions, allylic substitutions, and conjugate additions. This makes it essential for the synthesis of enantiomerically pure intermediates in the pharmaceutical industry, particularly for producing chiral active pharmaceutical ingredients (APIs) and complex natural products. Its specificity and efficiency in stereocontrol also extend to applications in fine chemical manufacturing and materials science where optical purity is required.

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Test Parameter Specification
Melting Point 215-225
Purity (HPLC) 98-100
Purity (With Total Nitrogen) 97.5-102.5
Specific Rotation 350-370
Specific Rotation 350-370
Appearance WHITE TO OFF-WHITE POWDER OR CRYSTALS
Infrared Spectrum Conforms to Structure
NMR (1H-NMR) Complies
Solubility in Dichloromethane Very faint turbidity

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,140.00
inventory 250mg
10-20 days ฿2,320.00
inventory 1g
10-20 days ฿6,180.00

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[3aR-[2(3'aR*,8'aS*),3'aβ,8'aβ]]-()-2,2'-Methylenebis[3a,8a-dihydro-8H-indeno[1,2-d]oxazole]
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This chiral bis(oxazoline) ligand, featuring a rigid indeno-fused structure connected by a methylene bridge, is primarily utilized in asymmetric catalysis. It coordinates with transition metals such as copper, palladium, or ruthenium to enable highly enantioselective reactions, including Diels-Alder cycloadditions, aldol reactions, allylic substitutions, and conjugate additions. This makes it essential for the synthesis of enantiomerically pure intermediates in the pharmaceutical industry, particularly f

This chiral bis(oxazoline) ligand, featuring a rigid indeno-fused structure connected by a methylene bridge, is primarily utilized in asymmetric catalysis. It coordinates with transition metals such as copper, palladium, or ruthenium to enable highly enantioselective reactions, including Diels-Alder cycloadditions, aldol reactions, allylic substitutions, and conjugate additions. This makes it essential for the synthesis of enantiomerically pure intermediates in the pharmaceutical industry, particularly for producing chiral active pharmaceutical ingredients (APIs) and complex natural products. Its specificity and efficiency in stereocontrol also extend to applications in fine chemical manufacturing and materials science where optical purity is required.

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