1,3,5,7-Tetrabromo-2,6-naphthalenediol is a brominated organic compound characterized by the presence of four bromine atoms and two hydroxyl (–OH) groups attached to a naphthalene ring system. This compound typically exhibits a high degree of hydrophobicity due to the bromine substituents, which can influence its solubility in various solvents. The presence of hydroxyl groups imparts some degree of polarity, allowing for potential interactions with polar solvents. The compound is often studied for its biological activity, particularly in the context of its potential as a biocide or in other applications related to environmental chemistry. Its structure suggests that it may participate in hydrogen bonding, which can affect its reactivity and interactions with other chemical species. Additionally, the bromine atoms can enhance the compound's stability and resistance to degradation. Overall, 1,3,5,7-tetrabromo-2,6-naphthalenediol is of interest in both synthetic and applied chemistry due to its unique properties and potential applications.

1,3,5,7-tetrabromo-2,6-naphthalenediol

133546-43-7: 1,3,5,7-Tetrabromo-2,6-naphthalenediol is a brominated organic compound characterized by the presence of four bromine atoms and two hydroxyl (–OH) groups attached to a naphthalene ring system. This compound typically exhibits a high degree of hydrophobicity due to the bromine substituents, which can influence its solubility in various solvents. The presence of hydroxyl groups imparts some degree of polarity, allowing for potential interactions with polar solvents. The compound is often studied for its biological activity, particularly in the context of its potential as a biocide or in other applications related to environmental chemistry. Its structure suggests that it may participate in hydrogen bonding, which can affect its reactivity and interactions with other chemical species. Additionally, the bromine atoms can enhance the compound's stability and resistance to degradation. Overall, 1,3,5,7-tetrabromo-2,6-naphthalenediol is of interest in both synthetic and applied chemistry due to its unique properties and potential applications.

CAS 133546-43-7

1,3,5,7-tetrabromo-2,6-naphthalenediol

1,3,5,7-Tetrabromonaphthalene-2,6-diol

Ref: 54-OR1049781