(3-Iodo-5-nitrophenyl)methanol

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Reagent Code: #131801
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CAS Number 219589-42-1

science Other reagents with same CAS 219589-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.03 g/mol
Formula C₇H₆INO₃
badge Registry Numbers
MDL Number MFCD18397990
thermostat Physical Properties
Boiling Point 393.0±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.034±0.06 g/cm3(Predicted)
Storage 2-8°C, away from light, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and bioactive compounds. Its structure contains both iodo and nitro functional groups, making it suitable for cross-coupling reactions such as Suzuki or Heck reactions, where the iodo group acts as a reactive site. The nitro group can be reduced to an amine, enabling further derivatization for use in medicinal chemistry. The hydroxymethyl group provides an anchor point for attachment to polymers or other molecular scaffolds, useful in the development of probes or drug delivery systems. Commonly employed in the synthesis of antimicrobial agents and enzyme inhibitors due to the electron-withdrawing nature of the nitro group and the heavy atom effect from iodine, which can enhance biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,140.00
inventory 250mg
10-20 days ฿12,170.00
inventory 1g
10-20 days ฿26,260.00

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(3-Iodo-5-nitrophenyl)methanol
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Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and bioactive compounds. Its structure contains both iodo and nitro functional groups, making it suitable for cross-coupling reactions such as Suzuki or Heck reactions, where the iodo group acts as a reactive site. The nitro group can be reduced to an amine, enabling further derivatization for use in medicinal chemistry. The hydroxymethyl group provides an anchor point for attachment to polymers or ot

Used primarily as an intermediate in organic synthesis, especially in the preparation of pharmaceuticals and bioactive compounds. Its structure contains both iodo and nitro functional groups, making it suitable for cross-coupling reactions such as Suzuki or Heck reactions, where the iodo group acts as a reactive site. The nitro group can be reduced to an amine, enabling further derivatization for use in medicinal chemistry. The hydroxymethyl group provides an anchor point for attachment to polymers or other molecular scaffolds, useful in the development of probes or drug delivery systems. Commonly employed in the synthesis of antimicrobial agents and enzyme inhibitors due to the electron-withdrawing nature of the nitro group and the heavy atom effect from iodine, which can enhance biological activity.

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