2,6-Bis[(4S)-4-tert-butyloxazolin-2-yl]pyridine

97%

Reagent Code: #70603
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CAS Number 118949-63-6

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.4 g/mol
Formula C₁₉H₂₇N₃O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in organic synthesis. It plays a crucial role in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where precise control over stereochemistry is required. Its rigid structure and chiral oxazoline groups make it highly effective in coordinating with transition metals like palladium, rhodium, and iridium, enabling the production of enantiomerically pure compounds. These compounds are valuable in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) and in the production of fine chemicals. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore novel asymmetric reactions.

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Test Parameter Specification
Appearance White to off-white powder
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,260.00
inventory 500mg
10-20 days ฿5,980.00

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2,6-Bis[(4S)-4-tert-butyloxazolin-2-yl]pyridine
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in organic synthesis. It plays a crucial role in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where precise control over stereochemistry is required. Its rigid structure and chiral oxazoline groups make it highly effective in coordinating with transition metals like palladium, rhodium, and iridium, enabling the production of enantiomerically p

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in organic synthesis. It plays a crucial role in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where precise control over stereochemistry is required. Its rigid structure and chiral oxazoline groups make it highly effective in coordinating with transition metals like palladium, rhodium, and iridium, enabling the production of enantiomerically pure compounds. These compounds are valuable in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs) and in the production of fine chemicals. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore novel asymmetric reactions.

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