2-(Benzyloxy)-1-(2-fluorophenyl)ethanone

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Reagent Code: #42073
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CAS Number 1402742-11-3

science Other reagents with same CAS 1402742-11-3

blur_circular Chemical Specifications

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Weight 244.2609 g/mol
Formula C₁₅H₁₃FO₂
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description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and bioactive molecules. Its structure, featuring both a benzyloxy group and a fluorophenyl moiety, makes it a valuable building block for developing compounds with potential therapeutic applications. Specifically, it is often employed in the synthesis of molecules targeting neurological disorders, as the fluorophenyl group can enhance binding affinity to certain receptors in the brain. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,268.00
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2-(Benzyloxy)-1-(2-fluorophenyl)ethanone
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This compound is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and bioactive molecules. Its structure, featuring both a benzyloxy group and a fluorophenyl moiety, makes it a valuable building block for developing compounds with potential therapeutic applications. Specifically, it is often employed in the synthesis of molecules targeting neurological disorders, as the fluorophenyl group can enhance binding affinity to certain receptors in the br

This compound is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and bioactive molecules. Its structure, featuring both a benzyloxy group and a fluorophenyl moiety, makes it a valuable building block for developing compounds with potential therapeutic applications. Specifically, it is often employed in the synthesis of molecules targeting neurological disorders, as the fluorophenyl group can enhance binding affinity to certain receptors in the brain. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and development.

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