1-Bromo-3-(2,2,2-trifluoroethoxy)benzene is an organic compound characterized by its aromatic structure, featuring a bromine atom and a trifluoroethoxy group attached to a benzene ring. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and polarity. The trifluoroethoxy group, consisting of a trifluoroethyl moiety linked to an ether oxygen, imparts significant electronegativity and hydrophobic characteristics, making the compound less soluble in water but potentially more soluble in organic solvents. This compound is likely to exhibit interesting chemical behavior due to the combination of the electron-withdrawing trifluoroethyl group and the electron-donating nature of the aromatic system. It may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, depending on the reaction conditions. Additionally, the presence of fluorine atoms can enhance the compound's thermal stability and influence its interactions in biological systems, making it of interest in fields such as medicinal chemistry and materials science.

1-bromo-3-(2,2,2-trifluoroethoxy)benzene

888327-41-1: 1-Bromo-3-(2,2,2-trifluoroethoxy)benzene is an organic compound characterized by its aromatic structure, featuring a bromine atom and a trifluoroethoxy group attached to a benzene ring. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and polarity. The trifluoroethoxy group, consisting of a trifluoroethyl moiety linked to an ether oxygen, imparts significant electronegativity and hydrophobic characteristics, making the compound less soluble in water but potentially more soluble in organic solvents. This compound is likely to exhibit interesting chemical behavior due to the combination of the electron-withdrawing trifluoroethyl group and the electron-donating nature of the aromatic system. It may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, depending on the reaction conditions. Additionally, the presence of fluorine atoms can enhance the compound's thermal stability and influence its interactions in biological systems, making it of interest in fields such as medicinal chemistry and materials science.

1-Bromo-3-(2,2,2-trifluoroethoxy)benzene

<p>1-Bromo-3-(2,2,2-trifluoroethoxy)benzene</p>

CAS 888327-41-1

1-bromo-3-(2,2,2-trifluoroethoxy)benzene

1-Bromo-3-(2,2,2-trifluoroethoxy)benzene

Ref: IN-DA004AJ5

1-Bromo-3-(2,2,2-trifluoroethoxy)benzene

Ref: 54-PC7194

1-Bromo-3-(2,2,2-trifluoroethoxy)benzene

Ref: 10-F236201