2,2'-Isopropylidenebis[(4S)-4-tert-butyl-2-oxazoline]

95%

Reagent Code: #126741
label
Alias (S,S)-(-)-2,2'-Isopropylidenebis(4-tert-butyl-2-oxazoline)​​
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CAS Number 131833-93-7

science Other reagents with same CAS 131833-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.43 g/mol
Formula C₁₇H₃₀N₂O₂
badge Registry Numbers
MDL Number MFCD00192243
thermostat Physical Properties
Melting Point 89-91 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs, where the biological activity can be highly dependent on the correct chiral form. Additionally, it finds use in academic research for developing new methodologies in organic synthesis and exploring stereochemical outcomes in complex reactions.

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Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,650.00
inventory 250mg
10-20 days ฿2,490.00

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2,2'-Isopropylidenebis[(4S)-4-tert-butyl-2-oxazoline]
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceuti

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and stereochemical properties make it effective in controlling the spatial arrangement of reactants, leading to the formation of specific enantiomers. This is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs, where the biological activity can be highly dependent on the correct chiral form. Additionally, it finds use in academic research for developing new methodologies in organic synthesis and exploring stereochemical outcomes in complex reactions.

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