4-Iodo-3-nitrophenol is an organic compound characterized by the presence of both an iodine and a nitro group attached to a phenolic ring. Its molecular structure features a hydroxyl group (-OH) that contributes to its acidic properties, making it a weak acid. The iodine atom, being a halogen, introduces significant electronegativity, which influences the compound's reactivity and stability. The nitro group (-NO2) is a strong electron-withdrawing group, enhancing the compound's electrophilic character and making it useful in various chemical reactions, including nucleophilic substitutions. This compound is typically a solid at room temperature and may exhibit yellow to brown coloration, depending on its purity and form. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic aromatic structure. 4-Iodo-3-nitrophenol is often utilized in research and industrial applications, including as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Proper handling and safety measures are essential, as it may pose health risks upon exposure.

4-iodo-3-nitrophenol

3-Iodo-4-nitrophenol

3-Iodo-4-nitrophenol is a synthetically developed molecule that is used as an industrial chemical. It has been shown to inhibit the growth of bacteria by binding to bacterial DNA and inhibiting RNA synthesis. It also inhibits the production of indole alkaloids, which are important for plant metabolism. 3-Iodo-4-nitrophenol is a synthetic derivative of an arbidol hydrochloride molecule, which is an analog of the natural indole alkaloid molecule dimethylamine. The synthetic arbidol molecule can be synthesized from carbon tetrachloride, with catalysis by a metal such as iron or nickel.

CAS 50590-07-3: 4-iodo-3-nitrophenol

3-Iodo-4-nitrophenol

Ref: IN-DA0037SN

3-Iodo-4-nitrophenol

Ref: 10-F092857

3-Iodo-4-nitrophenol

Ref: 54-OR400409

3-Iodo-4-nitrophenol

Ref: 3D-FI157231