2,5-Difluoro-4-iodoaniline is an organic compound characterized by the presence of two fluorine atoms and one iodine atom attached to a benzene ring that also features an amino group (-NH2). This compound belongs to the class of anilines, which are derivatives of benzene with an amino group. The fluorine atoms are positioned at the 2 and 5 positions of the aromatic ring, while the iodine is located at the 4 position, contributing to its unique reactivity and properties. The presence of halogens, such as fluorine and iodine, can significantly influence the compound's electronic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound may exhibit interesting biological activities, making it a candidate for pharmaceutical applications. Its molecular structure suggests potential for use in materials science and organic synthesis, particularly in the development of functionalized compounds. As with many halogenated anilines, care should be taken regarding its handling and disposal due to potential toxicity and environmental impact.

2,5-Difluoro-4-iodoaniline

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2,5-Difluoro-4-iodoaniline is a coupler that is used in the production of 2,5-difluoro-4-nitroaniline. It is used in cyclic voltammetry to study nucleophilic attack. 2,5-Difluoro-4-iodoaniline also reacts with carbodiimides to form betaines and diffracts x-rays. This molecule has a nitrogen atom in its structure and can be analyzed by x-ray diffraction.

CAS 155906-13-1: 2,5-Difluoro-4-iodoaniline

2,5-Difluoro-4-iodoaniline

Ref: 3D-FGA90613

2,5-Difluoro-4-iodoaniline

Ref: 54-PC908027

2,5-Difluoro-4-iodoaniline

Ref: 10-F460590

Benzenamine, 2,5-difluoro-4-iodo-

Ref: IN-DA001OC7