4-Bromo-2,6-diiodoaniline is an organic compound characterized by the presence of bromine and iodine substituents on an aniline backbone. Specifically, it features a bromine atom at the para position (4) and two iodine atoms at the ortho positions (2 and 6) relative to the amino group (-NH2) on the benzene ring. This compound is typically a solid at room temperature and may exhibit a range of colors depending on its purity and crystalline form. It is likely to be insoluble or only slightly soluble in water, but may dissolve in organic solvents such as ethanol or acetone. The presence of halogens can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the halogen substituents, which can affect its behavior in biological systems or materials science applications. Safety precautions should be taken when handling this compound, as halogenated compounds can pose health risks.

4-bromo-2,6-diiodoaniline

89280-77-3: 4-Bromo-2,6-diiodoaniline is an organic compound characterized by the presence of bromine and iodine substituents on an aniline backbone. Specifically, it features a bromine atom at the para position (4) and two iodine atoms at the ortho positions (2 and 6) relative to the amino group (-NH2) on the benzene ring. This compound is typically a solid at room temperature and may exhibit a range of colors depending on its purity and crystalline form. It is likely to be insoluble or only slightly soluble in water, but may dissolve in organic solvents such as ethanol or acetone. The presence of halogens can influence its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the compound may exhibit interesting electronic properties due to the electron-withdrawing nature of the halogen substituents, which can affect its behavior in biological systems or materials science applications. Safety precautions should be taken when handling this compound, as halogenated compounds can pose health risks.

CAS 89280-77-3

4-bromo-2,6-diiodoaniline

4-Bromo-2,6-diiodoaniline

Ref: IN-DA003KVX

4-Bromo-2,6-diiodoaniline

Ref: 54-OR16464