4-Fluoro-5-nitrobenzene-1,2-diamine, with the CAS number 113269-06-0, is an organic compound characterized by the presence of both amino and nitro functional groups on a benzene ring. This compound features a fluorine atom at the para position relative to the nitro group, and two amino groups located at the ortho positions. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and materials science. The nitro group is known for its electron-withdrawing properties, which can influence the compound's reactivity in electrophilic aromatic substitution reactions. Additionally, the amino groups can participate in hydrogen bonding and can serve as sites for further chemical modifications. The compound's solubility, stability, and reactivity can vary depending on the solvent and conditions used. Safety data should be consulted for handling, as compounds with nitro and amino groups can pose health risks. Overall, 4-fluoro-5-nitrobenzene-1,2-diamine is a valuable compound for research and industrial applications.

4-FLUORO-5-NITROBENZENE-1,2-DIAMINE

113269-06-0: 1,2-Benzenediamine, 4-Fluoro-5-Nitro-,  4-FLUORO-5-NITROBENZENE-1,2-DIAMINE

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CAS 113269-06-0: 4-FLUORO-5-NITROBENZENE-1,2-DIAMINE

4-Fluoro-5-Nitro-1,2-Benzenediamine

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