4-(5-Methyl-1,2,4-oxadiazol-3-yl)phenol, with the CAS number 49787-02-2, is an organic compound characterized by the presence of a phenolic group and a 1,2,4-oxadiazole moiety. This compound typically exhibits properties such as moderate solubility in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The oxadiazole ring contributes to its potential biological activity, as such heterocycles are often associated with antimicrobial and antifungal properties. The methyl group on the oxadiazole enhances its lipophilicity, potentially influencing its interaction with biological membranes. Additionally, the compound may exhibit UV absorbance due to the conjugated system formed by the phenolic and oxadiazole structures, making it of interest in various applications, including pharmaceuticals and agrochemicals. Its stability and reactivity can be influenced by the presence of the hydroxyl group, which can participate in various chemical reactions, including oxidation and substitution. Overall, this compound's unique structural features contribute to its diverse potential applications in chemical and biological fields.

4-(5-methyl-1,2,4-oxadiazol-3-yl)phenol

49787-02-2: 4-(5-Methyl-1,2,4-oxadiazol-3-yl)phenol, with the CAS number 49787-02-2, is an organic compound characterized by the presence of a phenolic group and a 1,2,4-oxadiazole moiety. This compound typically exhibits properties such as moderate solubility in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The oxadiazole ring contributes to its potential biological activity, as such heterocycles are often associated with antimicrobial and antifungal properties. The methyl group on the oxadiazole enhances its lipophilicity, potentially influencing its interaction with biological membranes. Additionally, the compound may exhibit UV absorbance due to the conjugated system formed by the phenolic and oxadiazole structures, making it of interest in various applications, including pharmaceuticals and agrochemicals. Its stability and reactivity can be influenced by the presence of the hydroxyl group, which can participate in various chemical reactions, including oxidation and substitution. Overall, this compound's unique structural features contribute to its diverse potential applications in chemical and biological fields.

CAS 49787-02-2

4-(5-methyl-1,2,4-oxadiazol-3-yl)phenol

4-(5-Methyl-1,2,4-oxadiazol-3-yl)phenol

Ref: IN-DA00DBGO

4-(5-Methyl-1,2,4-oxadiazol-3-yl)phenol

Ref: 54-OR82462

4-(5-methyl-1,2,4-oxadiazol-3-yl)phenol

Ref: 10-F310441