Methyl 3-(4-[(2-fluorobenzoyl)amino]phenoxy)-2-thiophenecarboxylate, identified by its CAS number 900019-25-2, is a synthetic organic compound characterized by its complex molecular structure, which includes a thiophene ring, a carboxylate group, and a fluorobenzoyl amino group. This compound typically exhibits properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many thiophene derivatives. Its structure suggests potential biological activity, making it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. The presence of the fluorobenzoyl moiety may enhance its lipophilicity and biological interactions. Additionally, the compound may undergo various chemical reactions, including esterification and nucleophilic substitutions, due to the functional groups present. As with many synthetic compounds, safety data and handling precautions should be considered, as they may pose risks depending on exposure levels. Overall, this compound represents a unique class of chemical entities with potential applications in medicinal chemistry.

METHYL 3-(4-[(2-FLUOROBENZOYL)AMINO]PHENOXY)-2-THIOPHENECARBOXYLATE

900019-25-2: Methyl 3-(4-[(2-fluorobenzoyl)amino]phenoxy)-2-thiophenecarboxylate, identified by its CAS number 900019-25-2, is a synthetic organic compound characterized by its complex molecular structure, which includes a thiophene ring, a carboxylate group, and a fluorobenzoyl amino group. This compound typically exhibits properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many thiophene derivatives. Its structure suggests potential biological activity, making it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. The presence of the fluorobenzoyl moiety may enhance its lipophilicity and biological interactions. Additionally, the compound may undergo various chemical reactions, including esterification and nucleophilic substitutions, due to the functional groups present. As with many synthetic compounds, safety data and handling precautions should be considered, as they may pose risks depending on exposure levels. Overall, this compound represents a unique class of chemical entities with potential applications in medicinal chemistry.

CAS 900019-25-2

METHYL 3-(4-[(2-FLUOROBENZOYL)AMINO]PHENOXY)-2-THIOPHENECARBOXYLATE