4'-(Trifluoromethoxy)biphenyl-2-carbaldehyde is an organic compound characterized by its biphenyl structure, which consists of two phenyl rings connected by a single bond. The presence of a trifluoromethoxy group (-O-CF3) at the para position of one phenyl ring significantly influences its chemical properties, including its reactivity and polarity. The aldehyde functional group (-CHO) located at the 2-position of the biphenyl moiety contributes to its potential as a reactive intermediate in various chemical reactions, such as nucleophilic additions. This compound is likely to exhibit unique electronic properties due to the electron-withdrawing nature of the trifluoromethoxy group, which can enhance its electrophilicity. Additionally, the presence of fluorine atoms can impart increased stability and lipophilicity, making it of interest in medicinal chemistry and materials science. Its specific applications may include use in the synthesis of pharmaceuticals or as a building block in organic synthesis. Safety data and handling precautions should be considered, as with any chemical substance, particularly those containing halogens.

4'-(trifluoromethoxy)biphenyl-2-carbaldehyde

728919-13-9: 4'-(Trifluoromethoxy)biphenyl-2-carbaldehyde is an organic compound characterized by its biphenyl structure, which consists of two phenyl rings connected by a single bond. The presence of a trifluoromethoxy group (-O-CF3) at the para position of one phenyl ring significantly influences its chemical properties, including its reactivity and polarity. The aldehyde functional group (-CHO) located at the 2-position of the biphenyl moiety contributes to its potential as a reactive intermediate in various chemical reactions, such as nucleophilic additions. This compound is likely to exhibit unique electronic properties due to the electron-withdrawing nature of the trifluoromethoxy group, which can enhance its electrophilicity. Additionally, the presence of fluorine atoms can impart increased stability and lipophilicity, making it of interest in medicinal chemistry and materials science. Its specific applications may include use in the synthesis of pharmaceuticals or as a building block in organic synthesis. Safety data and handling precautions should be considered, as with any chemical substance, particularly those containing halogens.

CAS 728919-13-9

4'-(trifluoromethoxy)biphenyl-2-carbaldehyde

4′-Trifluoromethoxy-biphenyl-2-carbaldehyde

Ref: 10-F020832