4-Iodo-2-nitrophenol

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Reagent Code: #200547
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CAS Number 21784-73-6

science Other reagents with same CAS 21784-73-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.01 g/mol
Formula C₆H₄INO₃
badge Registry Numbers
MDL Number MFCD00466297
inventory_2 Storage & Handling
Storage 2-8°C, store away from light, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of nitrophenol-based active ingredients. It serves in the development of certain antimicrobial compounds due to the combined effect of nitro and iodo functional groups. Also employed in organic research for halogenation studies and as a building block in cross-coupling reactions, such as Suzuki or Heck reactions, to construct complex aromatic molecules. Its structure allows for selective derivatization, making it valuable in medicinal chemistry for modifying bioactive molecules.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,960.00
inventory 10g
10-20 days ฿9,860.00
inventory 25g
10-20 days ฿18,550.00

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4-Iodo-2-nitrophenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of nitrophenol-based active ingredients. It serves in the development of certain antimicrobial compounds due to the combined effect of nitro and iodo functional groups. Also employed in organic research for halogenation studies and as a building block in cross-coupling reactions, such as Suzuki or Heck reactions, to construct complex aromatic molecules. Its structure allows for selective derivat

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of nitrophenol-based active ingredients. It serves in the development of certain antimicrobial compounds due to the combined effect of nitro and iodo functional groups. Also employed in organic research for halogenation studies and as a building block in cross-coupling reactions, such as Suzuki or Heck reactions, to construct complex aromatic molecules. Its structure allows for selective derivatization, making it valuable in medicinal chemistry for modifying bioactive molecules.

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