Methyl 4-fluoro-3-iodobenzoate

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Reagent Code: #46876
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CAS Number 1121586-29-5

science Other reagents with same CAS 1121586-29-5

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Weight 280.0349 g/mol
Formula C₈H₆FIO₂
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MDL Number MFCD11870177
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This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for developing active pharmaceutical ingredients (APIs). The presence of both fluorine and iodine atoms makes it a useful substrate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating carbon-carbon bonds in drug discovery. Additionally, its ester group allows for further functionalization, enabling the synthesis of a wide range of derivatives with potential biological activity. It is also employed in material science for the development of specialty chemicals and advanced materials.

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inventory 250mg
10-20 days ฿1,188.00

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Methyl 4-fluoro-3-iodobenzoate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for developing active pharmaceutical ingredients (APIs). The presence of both fluorine and iodine atoms makes it a useful substrate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating carbon-carbon bonds in drug discovery. Additionally, it

This compound is primarily utilized in organic synthesis as a versatile intermediate for constructing more complex molecules. It is particularly valuable in pharmaceutical research, where it serves as a building block for developing active pharmaceutical ingredients (APIs). The presence of both fluorine and iodine atoms makes it a useful substrate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating carbon-carbon bonds in drug discovery. Additionally, its ester group allows for further functionalization, enabling the synthesis of a wide range of derivatives with potential biological activity. It is also employed in material science for the development of specialty chemicals and advanced materials.

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