1-(2-Fluoro-5-iodophenyl)ethanone

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Reagent Code: #82188
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CAS Number 1159512-66-9

science Other reagents with same CAS 1159512-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.04 g/mol
Formula C₈H₆FIO
badge Registry Numbers
MDL Number MFCD12026480
inventory_2 Storage & Handling
Storage Room temperature, dark, inert gas storage

description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure, featuring both a fluoro and an iodo substituent, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and material science research. Additionally, the presence of the ethanone group allows for further functionalization, making it a useful intermediate in the synthesis of heterocyclic compounds, which are often explored for their potential biological activities. Its applications extend to the development of agrochemicals and dyes, where its unique reactivity can be leveraged to create targeted products.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,555.00
inventory 100mg
10-20 days ฿1,845.00

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1-(2-Fluoro-5-iodophenyl)ethanone
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This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure, featuring both a fluoro and an iodo substituent, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and material science research. Additionally, the presence of the ethanone group allows for further functionalization, making it a useful intermediate in the synthesis of he

This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its structure, featuring both a fluoro and an iodo substituent, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in pharmaceutical and material science research. Additionally, the presence of the ethanone group allows for further functionalization, making it a useful intermediate in the synthesis of heterocyclic compounds, which are often explored for their potential biological activities. Its applications extend to the development of agrochemicals and dyes, where its unique reactivity can be leveraged to create targeted products.

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