(S)-4-Benzyl-2-(isoquinolin-1-yl)-4,5-dihydrooxazole

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Reagent Code: #38543
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CAS Number 2058236-52-3

science Other reagents with same CAS 2058236-52-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.3431 g/mol
Formula C₁₉H₁₆N₂O
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its structure, featuring a dihydrooxazole ring and an isoquinoline moiety, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the pharmaceutical industry to synthesize chiral intermediates for drug development, ensuring high enantiomeric purity. Additionally, it finds use in academic research for studying stereochemistry and developing new catalytic methodologies. Its stability and selectivity make it a valuable tool in the synthesis of complex organic molecules.

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inventory 100mg
10-20 days ฿1,719.00

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(S)-4-Benzyl-2-(isoquinolin-1-yl)-4,5-dihydrooxazole
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its structure, featuring a dihydrooxazole ring and an isoquinoline moiety, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the pharmaceutical industry to synthesize chiral intermediates for drug development, ensuring high enantiomeric purity. Additionally, it f

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its structure, featuring a dihydrooxazole ring and an isoquinoline moiety, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. It is often employed in the pharmaceutical industry to synthesize chiral intermediates for drug development, ensuring high enantiomeric purity. Additionally, it finds use in academic research for studying stereochemistry and developing new catalytic methodologies. Its stability and selectivity make it a valuable tool in the synthesis of complex organic molecules.

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