2,6-Dichloro-3,5-difluorophenol is an organic compound characterized by its aromatic structure, which includes a phenolic hydroxyl group (-OH) and multiple halogen substituents. Specifically, it features two chlorine atoms at the 2 and 6 positions and two fluorine atoms at the 3 and 5 positions of the phenol ring. This compound is typically a solid at room temperature and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of both chlorine and fluorine atoms contributes to its chemical stability and reactivity, influencing its solubility and interaction with biological systems. Additionally, the compound may exhibit unique properties such as antimicrobial activity or serve as an intermediate in the synthesis of more complex molecules. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, 2,6-dichloro-3,5-difluorophenol is a notable example of a halogenated phenolic compound with diverse potential applications.

2,6-dichloro-3,5-difluorophenol

63418-08-6: 2,6-Dichloro-3,5-difluorophenol is an organic compound characterized by its aromatic structure, which includes a phenolic hydroxyl group (-OH) and multiple halogen substituents. Specifically, it features two chlorine atoms at the 2 and 6 positions and two fluorine atoms at the 3 and 5 positions of the phenol ring. This compound is typically a solid at room temperature and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of both chlorine and fluorine atoms contributes to its chemical stability and reactivity, influencing its solubility and interaction with biological systems. Additionally, the compound may exhibit unique properties such as antimicrobial activity or serve as an intermediate in the synthesis of more complex molecules. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, 2,6-dichloro-3,5-difluorophenol is a notable example of a halogenated phenolic compound with diverse potential applications.

CAS 63418-08-6

2,6-dichloro-3,5-difluorophenol

2,6-Dichloro-3,5-difluorophenol

Ref: IN-DA00IB7J

2,6-Dichloro-3,5-difluorophenol

Ref: 54-PC4813

2,6-Dichloro-3,5-difluorophenol

Ref: 10-F010445