2-(Trifluoromethylthio)benzaldehyde is an organic compound characterized by the presence of a benzaldehyde functional group attached to a benzene ring, which is further substituted with a trifluoromethylthio group. This compound features a sulfur atom bonded to a trifluoromethyl group (–CF3), which significantly influences its chemical properties, including its reactivity and polarity. The trifluoromethylthio group is known for imparting unique electronic characteristics, making the compound a potential candidate for various applications in organic synthesis and medicinal chemistry. The presence of the aldehyde functional group allows for typical reactivity associated with aldehydes, such as nucleophilic addition reactions. Additionally, the trifluoromethylthio substituent can enhance the lipophilicity and stability of the compound, potentially affecting its biological activity. 2-(Trifluoromethylthio)benzaldehyde is typically handled with care due to the presence of fluorinated groups, which can pose environmental and health risks. Overall, this compound is of interest in the field of synthetic organic chemistry and may serve as a building block for more complex molecules.

2-(trifluoromethylthio)benzaldehyde

57830-48-5: 2-(Trifluoromethylthio)benzaldehyde is an organic compound characterized by the presence of a benzaldehyde functional group attached to a benzene ring, which is further substituted with a trifluoromethylthio group. This compound features a sulfur atom bonded to a trifluoromethyl group (–CF3), which significantly influences its chemical properties, including its reactivity and polarity. The trifluoromethylthio group is known for imparting unique electronic characteristics, making the compound a potential candidate for various applications in organic synthesis and medicinal chemistry. The presence of the aldehyde functional group allows for typical reactivity associated with aldehydes, such as nucleophilic addition reactions. Additionally, the trifluoromethylthio substituent can enhance the lipophilicity and stability of the compound, potentially affecting its biological activity. 2-(Trifluoromethylthio)benzaldehyde is typically handled with care due to the presence of fluorinated groups, which can pose environmental and health risks. Overall, this compound is of interest in the field of synthetic organic chemistry and may serve as a building block for more complex molecules.

CAS 57830-48-5

2-(trifluoromethylthio)benzaldehyde

2-[(Trifluoromethyl)thio]benzaldehyde

Ref: 54-PC5544

2-(Trifluoromethylthio)benzaldehyde

Ref: 10-F007994