Ethyl 5-(3-methoxyphenyl)-1H-pyrazole-3-carboxylate is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a 3-methoxyphenyl substituent enhances its potential for biological activity, as aromatic rings often play a crucial role in interactions with biological targets. The carboxylate group is known for its ability to participate in various chemical reactions, including esterification and amidation. Ethyl 5-(3-methoxyphenyl)-1H-pyrazole-3-carboxylate may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas targeting inflammation or other diseases where pyrazole derivatives have shown efficacy. As with many organic compounds, its stability, reactivity, and biological activity can be influenced by environmental factors such as pH and temperature.

ethyl 5-(3-methoxyphenyl)-1H-pyrazole-3-carboxylate

723339-63-7: Ethyl 5-(3-methoxyphenyl)-1H-pyrazole-3-carboxylate is a chemical compound characterized by its pyrazole core, which is a five-membered ring containing two nitrogen atoms. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of a 3-methoxyphenyl substituent enhances its potential for biological activity, as aromatic rings often play a crucial role in interactions with biological targets. The carboxylate group is known for its ability to participate in various chemical reactions, including esterification and amidation. Ethyl 5-(3-methoxyphenyl)-1H-pyrazole-3-carboxylate may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its molecular structure suggests potential applications in drug development, particularly in areas targeting inflammation or other diseases where pyrazole derivatives have shown efficacy. As with many organic compounds, its stability, reactivity, and biological activity can be influenced by environmental factors such as pH and temperature.

CAS 723339-63-7

ethyl 5-(3-methoxyphenyl)-1H-pyrazole-3-carboxylate

Ethyl 3-(3-methoxyphenyl)pyrazole-5-carboxylate

Ref: IN-DA0067FG

ETHYL 3-(3-METHOXYPHENYL)-1H-PYRAZOLE-5-CARBOXYLATE

Ref: 10-F388551