26 Diiodo 4 Nitrophenol
26 Diiodo 4 Nitrophenol is a specialized organic compound that serves as an important reagent in various chemical applications, particularly in the fields of organic synthesis and analytical chemistry. This compound is characterized by the presence of two iodine atoms and a nitro group attached to a phenolic ring, which significantly influences its chemical properties and reactivity.
The incorporation of iodine into the molecular structure enhances the compound’s electrophilic character, making it a valuable intermediate in the synthesis of complex organic molecules. It is often used as a building block in the preparation of pharmaceuticals, agrochemicals, and other functional materials. The nitro group contributes to its reactivity and can facilitate various chemical transformations, making it an essential compound for researchers and chemists.
26 Diiodo 4 Nitrophenol is also noted for its utility in analytical techniques, including spectroscopy and chromatography, where it may be employed as a marker or indicator in specific chemical reactions. Its distinctive structure allows for precise identification and quantification in mixtures, thus playing a crucial role in quality control and research applications.
Furthermore, this compound demonstrates interesting biological activities, which may warrant further exploration in pharmacological studies. Researchers continue to investigate its potential implications in various biological systems, highlighting its versatility as a chemical entity.
In summary, 26 Diiodo 4 Nitrophenol is a significant organic compound with wide-ranging applications in synthetic and analytical chemistry. Its unique structure, characterized by diiodo and nitro substituents, enhances its utility as a reagent and building block in the development of new chemical entities.
26 Diiodo 4 Nitrophenol | |
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Product Name | 26 Diiodo 4 Nitrophenol |
CAS No | 102-75-0 |
Molecular Formula | C₆H₂I₂N₂O₃ |
Molecular Weight | 308.88 g/mol |
Short Description | 26 Diiodo 4 Nitrophenol is an organic compound used primarily in organic synthesis and analytical chemistry. Its unique structure enhances its reactivity and utility in the synthesis of pharmaceuticals and agrochemicals. |
Identification by Chemical Test |
Test A: Dissolve in ethanol; the formation of a yellowish-brown solution indicates the presence of 26 Diiodo 4 Nitrophenol. Test B: React with sodium hydroxide; a distinct color change confirms the compound’s presence. Test C: Infrared spectroscopy displays characteristic peaks corresponding to the functional groups of 26 Diiodo 4 Nitrophenol. |
pH | 5.0 – 7.0 |
Loss on Drying | ≤ 5.0% |