5-[4-Chloro-3-(trifluoromethyl)phenyl]furan-2-carbaldehyde is an organic compound characterized by its furan and aldehyde functional groups, along with a chlorinated and trifluoromethyl-substituted phenyl ring. The presence of the furan ring contributes to its aromatic properties, while the aldehyde group indicates it can participate in various chemical reactions, such as nucleophilic additions. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. The chlorinated phenyl moiety may also impart unique electronic properties, making it of interest in medicinal chemistry and material science. This compound is typically used in research and development, particularly in the synthesis of more complex molecules or as an intermediate in organic synthesis. Its specific physical properties, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which it is studied. Safety data should be consulted, as halogenated compounds can exhibit toxicity and environmental persistence.

5-[4-chloro-3-(trifluoromethyl)phenyl]furan-2-carbaldehyde

58110-58-0: 5-[4-Chloro-3-(trifluoromethyl)phenyl]furan-2-carbaldehyde is an organic compound characterized by its furan and aldehyde functional groups, along with a chlorinated and trifluoromethyl-substituted phenyl ring. The presence of the furan ring contributes to its aromatic properties, while the aldehyde group indicates it can participate in various chemical reactions, such as nucleophilic additions. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and biological activity. The chlorinated phenyl moiety may also impart unique electronic properties, making it of interest in medicinal chemistry and material science. This compound is typically used in research and development, particularly in the synthesis of more complex molecules or as an intermediate in organic synthesis. Its specific physical properties, such as melting point, boiling point, and solubility, would depend on the molecular interactions and the environment in which it is studied. Safety data should be consulted, as halogenated compounds can exhibit toxicity and environmental persistence.

5-[4-Chloro-3-(trifluoromethyl)phenyl]-2-furaldehyde

CAS 58110-58-0

5-[4-chloro-3-(trifluoromethyl)phenyl]furan-2-carbaldehyde

5-[4-Chloro-3-(trifluoromethyl)phenyl]-2-furaldehyde

Ref: 54-PC101774

5-[4-Chloro-3-(trifluoromethyl)phenyl]-2-furaldehyde

Ref: 10-F618082