1-(4-Chloro-3-methylphenyl)-2,2,2-trifluoroethanone, with the CAS number 286017-71-8, is an organic compound characterized by its unique structure, which includes a trifluoroethanone moiety and a substituted phenyl group. This compound typically exhibits a high degree of lipophilicity due to the presence of the trifluoromethyl group, which can influence its solubility and reactivity. The chloro and methyl substitutions on the phenyl ring can affect its electronic properties, potentially enhancing its reactivity in electrophilic aromatic substitution reactions. The trifluoroethanone functional group is known for its strong electron-withdrawing properties, which can stabilize certain intermediates during chemical reactions. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its physical properties, such as boiling point, melting point, and density, would depend on the specific molecular interactions and the presence of functional groups. Overall, this compound's unique characteristics make it a subject of interest in both synthetic organic chemistry and medicinal chemistry.

1-(4-chloro-3-methylphenyl)-2,2,2-trifluoroethanone

286017-71-8: 1-(4-Chloro-3-methylphenyl)-2,2,2-trifluoroethanone, with the CAS number 286017-71-8, is an organic compound characterized by its unique structure, which includes a trifluoroethanone moiety and a substituted phenyl group. This compound typically exhibits a high degree of lipophilicity due to the presence of the trifluoromethyl group, which can influence its solubility and reactivity. The chloro and methyl substitutions on the phenyl ring can affect its electronic properties, potentially enhancing its reactivity in electrophilic aromatic substitution reactions. The trifluoroethanone functional group is known for its strong electron-withdrawing properties, which can stabilize certain intermediates during chemical reactions. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its physical properties, such as boiling point, melting point, and density, would depend on the specific molecular interactions and the presence of functional groups. Overall, this compound's unique characteristics make it a subject of interest in both synthetic organic chemistry and medicinal chemistry.

CAS 286017-71-8

1-(4-chloro-3-methylphenyl)-2,2,2-trifluoroethanone

1-(4-chloro-3-methylphenyl)-2,2,2-trifluoroethan-1-one

Ref: IN-DA002VU5

4'-Chloro-3'-methyl-2,2,2-trifluoroacetophenone

Ref: 54-PC2819

4′-Chloro-3′-methyl-2,2,2-trifluoroacetophenone

Ref: 10-F023167