(4S,4'S)-2,2'-(Pentane-3,3'-diyl)bis(4-benzyl-4,5-dihydrooxazole)

98.0%

Reagent Code: #69728
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CAS Number 160191-64-0

science Other reagents with same CAS 160191-64-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 390.53 g/mol
Formula C₂₅H₃₀N₂O₂
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, where it helps in the formation of chiral centers with high enantiomeric excess. Its structure, featuring a bis(oxazoline) framework, makes it effective in coordinating with metals like copper, palladium, and rhodium, enhancing the efficiency and selectivity of the catalytic system. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Its robust and tunable nature allows for its use in a variety of complex organic transformations.

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Test Parameter Specification
Appearance Pale yellow - deep yellow liquid
Purity 98-100
Specific Rotation (20°C, c=2.5, CHCl3) -23 to -20
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿5,580.00
inventory 1g
10-20 days ฿22,005.00

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(4S,4'S)-2,2'-(Pentane-3,3'-diyl)bis(4-benzyl-4,5-dihydrooxazole)
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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, where it helps in the formation of chiral centers with high enantiomeric excess. Its structure, featuring a bis(oxazoline) framework, makes it effective in coordinating with metals like copper, palladium, and rhodium, enhancing the efficiency and selectivity of the catal

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, where it helps in the formation of chiral centers with high enantiomeric excess. Its structure, featuring a bis(oxazoline) framework, makes it effective in coordinating with metals like copper, palladium, and rhodium, enhancing the efficiency and selectivity of the catalytic system. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Its robust and tunable nature allows for its use in a variety of complex organic transformations.

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