6-(4-Methoxy-3,5-dimethyl-phenyl)-6-oxo-hexanoic acid, with the CAS number 122004-99-3, is an organic compound characterized by its complex structure, which includes a hexanoic acid backbone and a substituted aromatic ring. The presence of the methoxy group and the dimethyl substitutions on the phenyl ring contribute to its unique chemical properties, such as increased lipophilicity and potential biological activity. This compound features a ketone functional group (6-oxo) that may influence its reactivity and interactions in various chemical environments. It is likely to exhibit moderate solubility in organic solvents due to its hydrophobic aromatic components, while the carboxylic acid group can engage in hydrogen bonding, affecting its solubility in polar solvents. The compound may also participate in various chemical reactions typical of carboxylic acids and ketones, such as esterification or condensation reactions. Its specific applications and biological activities would depend on further research and characterization, making it of interest in fields such as medicinal chemistry and organic synthesis.

6-(4-methoxy-3,5-dimethyl-phenyl)-6-oxo-hexanoic acid

122004-99-3: 6-(4-Methoxy-3,5-dimethyl-phenyl)-6-oxo-hexanoic acid, with the CAS number 122004-99-3, is an organic compound characterized by its complex structure, which includes a hexanoic acid backbone and a substituted aromatic ring. The presence of the methoxy group and the dimethyl substitutions on the phenyl ring contribute to its unique chemical properties, such as increased lipophilicity and potential biological activity. This compound features a ketone functional group (6-oxo) that may influence its reactivity and interactions in various chemical environments. It is likely to exhibit moderate solubility in organic solvents due to its hydrophobic aromatic components, while the carboxylic acid group can engage in hydrogen bonding, affecting its solubility in polar solvents. The compound may also participate in various chemical reactions typical of carboxylic acids and ketones, such as esterification or condensation reactions. Its specific applications and biological activities would depend on further research and characterization, making it of interest in fields such as medicinal chemistry and organic synthesis.

CAS 122004-99-3

6-(4-methoxy-3,5-dimethyl-phenyl)-6-oxo-hexanoic acid

Benzenehexanoic acid, 4-methoxy-3,5-dimethyl-ε-oxo-

Ref: IN-DA0016M5

6-(3,5-Dimethyl-4-methoxyphenyl)-6-oxohexanoic acid

Ref: 10-F207118