()-2,2'-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline]

96%

Reagent Code: #126740
label
Alias (R,R)-2,2'-Isopropylidene bis(4-phenyl-2-oxazoline)
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CAS Number 150529-93-4

science Other reagents with same CAS 150529-93-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.41 g/mol
Formula C₂₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD00192244
thermostat Physical Properties
Melting Point 56-58 °C(lit.)
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, to produce optically active compounds. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds applications in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is essential. Its stability and ability to form complexes with various transition metals further enhance its utility in organic synthesis.

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Test Parameter Specification
Purity (GC) 95.5-100%
Specific Rotation 155-165
Specific Rotation 155-165
Appearance Light yellow to yellow liquid or solid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,600.00

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()-2,2'-Isopropylidenebis[(4R)-4-phenyl-2-oxazoline]
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, to produce optically active compounds. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds applications in the synthesis of pharmac

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, cyclopropanation, and carbon-carbon bond-forming reactions, to produce optically active compounds. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds applications in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is essential. Its stability and ability to form complexes with various transition metals further enhance its utility in organic synthesis.

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