(S)-4-((S)-sec-Butyl)-2-(pyridin-2-yl)-4,5-dihydrooxazole

98%

Reagent Code: #123728
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CAS Number 108915-03-3

science Other reagents with same CAS 108915-03-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.27 g/mol
Formula C₁₂H₁₆N₂O
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis and catalysis, where it serves as a chiral ligand. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed reactions. It is often employed in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes, enhancing the production of chiral molecules with high optical purity. Its application is significant in pharmaceutical synthesis, where precise control over stereochemistry is crucial for the development of active pharmaceutical ingredients (APIs). Additionally, it is explored in materials science for designing chiral catalysts and frameworks.

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inventory 100mg
10-20 days ฿4,797.00

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(S)-4-((S)-sec-Butyl)-2-(pyridin-2-yl)-4,5-dihydrooxazole
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This compound is primarily utilized in the field of asymmetric synthesis and catalysis, where it serves as a chiral ligand. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed reactions. It is often employed in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes, enhancing the production of chiral molecules with high opti

This compound is primarily utilized in the field of asymmetric synthesis and catalysis, where it serves as a chiral ligand. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed reactions. It is often employed in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes, enhancing the production of chiral molecules with high optical purity. Its application is significant in pharmaceutical synthesis, where precise control over stereochemistry is crucial for the development of active pharmaceutical ingredients (APIs). Additionally, it is explored in materials science for designing chiral catalysts and frameworks.

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