[2,5-Dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]acetic acid is a chemical compound characterized by its unique pyrrole structure, which features a five-membered aromatic ring containing nitrogen. This compound includes two methyl groups at the 2 and 5 positions of the pyrrole ring, enhancing its lipophilicity and potentially influencing its biological activity. The presence of a 4-methylphenyl group at the 1-position contributes to its aromatic character and may affect its interactions with biological targets. The acetic acid functional group at the 3-position introduces acidity and polar characteristics, which can enhance solubility in polar solvents. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas where pyrrole derivatives are known to exhibit activity. As with many organic compounds, its stability, reactivity, and potential applications would depend on specific conditions such as pH, temperature, and the presence of other chemical species.

[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]acetic acid

42779-84-0: [2,5-Dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]acetic acid is a chemical compound characterized by its unique pyrrole structure, which features a five-membered aromatic ring containing nitrogen. This compound includes two methyl groups at the 2 and 5 positions of the pyrrole ring, enhancing its lipophilicity and potentially influencing its biological activity. The presence of a 4-methylphenyl group at the 1-position contributes to its aromatic character and may affect its interactions with biological targets. The acetic acid functional group at the 3-position introduces acidity and polar characteristics, which can enhance solubility in polar solvents. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas where pyrrole derivatives are known to exhibit activity. As with many organic compounds, its stability, reactivity, and potential applications would depend on specific conditions such as pH, temperature, and the presence of other chemical species.

CAS 42779-84-0

[2,5-dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]acetic acid

2-[2,5-Dimethyl-1-(4-methylphenyl)-1H-pyrrol-3-yl]acetic acid

Ref: 3D-SBA77984