
CAS 13116-27-3
:4-Iodophenylhydrazine
Description:
4-Iodophenylhydrazine is an organic compound characterized by the presence of a hydrazine functional group attached to a phenyl ring that is substituted with an iodine atom at the para position. Its molecular formula is C6H7I N2, and it typically appears as a solid or crystalline substance. This compound is known for its reactivity, particularly in the formation of azo compounds and as a reagent in various organic synthesis reactions. It can participate in electrophilic aromatic substitution due to the electron-withdrawing nature of the iodine atom, which influences its chemical behavior. Additionally, 4-Iodophenylhydrazine may exhibit biological activity, making it of interest in medicinal chemistry and research. Safety precautions should be observed when handling this compound, as it may pose health risks, including potential toxicity. Proper storage conditions are also essential to maintain its stability and prevent degradation. Overall, 4-Iodophenylhydrazine serves as a valuable intermediate in organic synthesis and research applications.
Formula:C6H7IN2
InChI:InChI=1/C6H7IN2/c7-5-1-3-6(9-8)4-2-5/h1-4,9H,8H2
SMILES:c1cc(ccc1I)NN
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Found 5 products.
4-Iodophenylhydrazine, 95%
CAS:<p>It can be used in agrochemical, pharmaceutical and dyestuff field. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU refere</p>Formula:C6H7IN2Purity:95%Color and Shape:Yellow to dark brown to brown, Crystals or powder or crystalline powder or fused solidMolecular weight:234.04(4-Iodophenyl)hydrazine hydroiodide
CAS:Formula:C6H7IN2Purity:95%Color and Shape:SolidMolecular weight:234.03774-Iodophenylhydrazine
CAS:4-IodophenylhydrazineFormula:C6H7IN2Purity:98%Color and Shape: tan solidMolecular weight:234.03765g/mol(4-Iodophenyl)hydrazine hydroiodide
CAS:<p>(4-Iodophenyl)hydrazine hydroiodide is a synthetic compound that has shown anti-viral activity against HIV and cytomegalovirus. It also has anticancer properties and can be used to treat colon cancer. The compound binds to the nucleic acid in a number of ways, including by forming reversible covalent bonds with functional groups on the nucleic acid. These interactions are primarily due to its pyrazole ring and hydrazine moiety. (4-Iodophenyl)hydrazine hydroiodide is structurally similar to phenyldiazenyl, which exhibits photochromism and fluorescence properties. This similarity may account for the observed photochemical changes in the molecule when exposed to light.</p>Formula:C6H7IN2Purity:Min. 95%Molecular weight:234.04 g/mol




