1-((3S)-6-methyl-7-oxabicyclo[4,1,0]heptan-3-yl)ethanone

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Reagent Code: #39075
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CAS Number 203508-62-7

science Other reagents with same CAS 203508-62-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.21 g/mol
Formula C₉H₁₄O₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique bicyclic structure makes it a valuable intermediate in creating compounds with potential biological activity. It is often employed in asymmetric synthesis to produce chiral molecules, which are crucial in the production of enantiomerically pure drugs. Additionally, its reactivity allows for modifications that can lead to the discovery of new chemical entities with applications in medicinal chemistry. Researchers also explore its use in the design of catalysts and ligands for various chemical reactions, enhancing efficiency and selectivity in industrial processes.

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inventory 1g
10-20 days ฿43,200.00

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1-((3S)-6-methyl-7-oxabicyclo[4,1,0]heptan-3-yl)ethanone
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique bicyclic structure makes it a valuable intermediate in creating compounds with potential biological activity. It is often employed in asymmetric synthesis to produce chiral molecules, which are crucial in the production of enantiomerically pure drugs. Additionally, its reactivity allows for modifications that can lead to the discovery of new c

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique bicyclic structure makes it a valuable intermediate in creating compounds with potential biological activity. It is often employed in asymmetric synthesis to produce chiral molecules, which are crucial in the production of enantiomerically pure drugs. Additionally, its reactivity allows for modifications that can lead to the discovery of new chemical entities with applications in medicinal chemistry. Researchers also explore its use in the design of catalysts and ligands for various chemical reactions, enhancing efficiency and selectivity in industrial processes.

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