6-Bromo-5-iodopyridin-3-ol is a heterocyclic organic compound characterized by the presence of a pyridine ring substituted with bromine and iodine atoms, as well as a hydroxyl group. The molecular structure features a six-membered aromatic ring containing nitrogen, which contributes to its basicity and potential reactivity. The bromine and iodine substituents introduce significant steric and electronic effects, influencing the compound's reactivity and interactions with other molecules. This compound may exhibit properties typical of halogenated pyridines, such as increased lipophilicity and potential for nucleophilic substitution reactions. The hydroxyl group can participate in hydrogen bonding, enhancing solubility in polar solvents and affecting its biological activity. Due to these characteristics, 6-bromo-5-iodopyridin-3-ol may find applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. Its unique combination of halogen substituents and functional groups makes it a valuable compound for further research and development in various chemical applications.

6-bromo-5-iodopyridin-3-ol

697300-70-2: 6-Bromo-5-iodopyridin-3-ol is a heterocyclic organic compound characterized by the presence of a pyridine ring substituted with bromine and iodine atoms, as well as a hydroxyl group. The molecular structure features a six-membered aromatic ring containing nitrogen, which contributes to its basicity and potential reactivity. The bromine and iodine substituents introduce significant steric and electronic effects, influencing the compound's reactivity and interactions with other molecules. This compound may exhibit properties typical of halogenated pyridines, such as increased lipophilicity and potential for nucleophilic substitution reactions. The hydroxyl group can participate in hydrogen bonding, enhancing solubility in polar solvents and affecting its biological activity. Due to these characteristics, 6-bromo-5-iodopyridin-3-ol may find applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. Its unique combination of halogen substituents and functional groups makes it a valuable compound for further research and development in various chemical applications.

CAS 697300-70-2

6-bromo-5-iodopyridin-3-ol

6-Bromo-5-iodopyridin-3-ol

Ref: IN-DA005UCP

2-Bromo-5-hydroxy-3-iodopyridine

Ref: 54-OR345396