Benzenebutanoic acid, α-methyl-γ-oxo-3-(trifluoromethyl)-, with the CAS number 66549-17-5, is an organic compound characterized by its complex structure that includes a benzenoid ring and a butanoic acid moiety. The presence of a trifluoromethyl group (-CF3) significantly influences its chemical properties, enhancing its lipophilicity and potentially affecting its reactivity and biological activity. The α-methyl and γ-oxo functional groups contribute to its unique reactivity, making it a candidate for various synthetic applications in organic chemistry. This compound may exhibit interesting interactions due to the electron-withdrawing nature of the trifluoromethyl group, which can stabilize certain reactive intermediates. Additionally, the presence of multiple functional groups suggests potential for diverse applications in pharmaceuticals, agrochemicals, or materials science. As with many organic compounds, its solubility, stability, and reactivity can be influenced by environmental conditions such as pH and temperature. Safety data should be consulted for handling and usage, as the trifluoromethyl group can also impart toxicity or environmental concerns.

Benzenebutanoic acid, a-methyl-g-oxo-3-(trifluoromethyl)-

66549-17-5: Benzenebutanoic acid, α-methyl-γ-oxo-3-(trifluoromethyl)-, with the CAS number 66549-17-5, is an organic compound characterized by its complex structure that includes a benzenoid ring and a butanoic acid moiety. The presence of a trifluoromethyl group (-CF3) significantly influences its chemical properties, enhancing its lipophilicity and potentially affecting its reactivity and biological activity. The α-methyl and γ-oxo functional groups contribute to its unique reactivity, making it a candidate for various synthetic applications in organic chemistry. This compound may exhibit interesting interactions due to the electron-withdrawing nature of the trifluoromethyl group, which can stabilize certain reactive intermediates. Additionally, the presence of multiple functional groups suggests potential for diverse applications in pharmaceuticals, agrochemicals, or materials science. As with many organic compounds, its solubility, stability, and reactivity can be influenced by environmental conditions such as pH and temperature. Safety data should be consulted for handling and usage, as the trifluoromethyl group can also impart toxicity or environmental concerns.

2-methyl-4-oxo-4-[3-(trifluoromethyl)phenyl]butanoic acid

<p>2-Methyl-4-oxo-4-[3-(trifluoromethyl)phenyl]butanoic acid</p>

CAS 66549-17-5

Benzenebutanoic acid, a-methyl-g-oxo-3-(trifluoromethyl)-

2-methyl-4-oxo-4-[3-(trifluoromethyl)phenyl]butanoic acid

Ref: IN-DA00IBM2

2-Methyl-4-oxo-4-[3-(trifluoromethyl)phenyl]butanoic acid

Ref: 54-PC8904