2-Bromo-3,6-difluorobenzyl alcohol is an organic compound characterized by its aromatic structure, which includes a benzyl alcohol moiety substituted with bromine and fluorine atoms. The presence of the bromine atom at the second position and two fluorine atoms at the third and sixth positions on the benzene ring significantly influences its chemical properties, including reactivity and polarity. This compound is likely to exhibit moderate solubility in polar solvents due to the hydroxyl (-OH) group, which can engage in hydrogen bonding. The fluorine substituents can enhance the compound's electronegativity, potentially affecting its interaction with other molecules and its overall stability. Additionally, the bromine atom may introduce unique reactivity patterns, making it a candidate for various chemical reactions, including nucleophilic substitutions. Due to its specific functional groups and substituents, 2-bromo-3,6-difluorobenzyl alcohol may find applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

2-bromo-3,6-difluorobenzyl alcohol

1404115-38-3: 2-Bromo-3,6-difluorobenzyl alcohol is an organic compound characterized by its aromatic structure, which includes a benzyl alcohol moiety substituted with bromine and fluorine atoms. The presence of the bromine atom at the second position and two fluorine atoms at the third and sixth positions on the benzene ring significantly influences its chemical properties, including reactivity and polarity. This compound is likely to exhibit moderate solubility in polar solvents due to the hydroxyl (-OH) group, which can engage in hydrogen bonding. The fluorine substituents can enhance the compound's electronegativity, potentially affecting its interaction with other molecules and its overall stability. Additionally, the bromine atom may introduce unique reactivity patterns, making it a candidate for various chemical reactions, including nucleophilic substitutions. Due to its specific functional groups and substituents, 2-bromo-3,6-difluorobenzyl alcohol may find applications in pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose health and environmental risks.

2-Bromo-3,6-difluorobenzyl alcohol

<p>2-Bromo-3,6-difluorobenzyl alcohol</p>

CAS 1404115-38-3

2-bromo-3,6-difluorobenzyl alcohol

2-Bromo-3,6-difluorobenzyl alcohol

Ref: IN-DA01FHA1

2-Bromo-3,6-difluorobenzyl alcohol

Ref: 54-PC501760

2-Bromo-3,6-difluorobenzyl alcohol

Ref: 10-F631293