5-(6-Methoxynaphthalen-2-yl)-1H-pyrazole is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of a methoxynaphthalene substituent at the 5-position of the pyrazole enhances its aromatic properties and may influence its biological activity. This compound typically exhibits moderate to high lipophilicity due to the naphthalene moiety, which can affect its solubility and permeability in biological systems. It may also display interesting pharmacological properties, making it a subject of interest in medicinal chemistry. The compound's structure suggests potential interactions with various biological targets, and it may be investigated for its role in drug development or as a chemical probe in research. Additionally, its synthesis and characterization involve standard organic chemistry techniques, including reactions that form the pyrazole ring and subsequent functionalization to introduce the methoxy group. Overall, 5-(6-methoxynaphthalen-2-yl)-1H-pyrazole represents a versatile scaffold for further exploration in chemical and pharmaceutical applications.

5-(6-methoxynaphthalen-2-yl)-1H-pyrazole

258518-56-8: 5-(6-Methoxynaphthalen-2-yl)-1H-pyrazole is an organic compound characterized by its pyrazole core, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of a methoxynaphthalene substituent at the 5-position of the pyrazole enhances its aromatic properties and may influence its biological activity. This compound typically exhibits moderate to high lipophilicity due to the naphthalene moiety, which can affect its solubility and permeability in biological systems. It may also display interesting pharmacological properties, making it a subject of interest in medicinal chemistry. The compound's structure suggests potential interactions with various biological targets, and it may be investigated for its role in drug development or as a chemical probe in research. Additionally, its synthesis and characterization involve standard organic chemistry techniques, including reactions that form the pyrazole ring and subsequent functionalization to introduce the methoxy group. Overall, 5-(6-methoxynaphthalen-2-yl)-1H-pyrazole represents a versatile scaffold for further exploration in chemical and pharmaceutical applications.

CAS 258518-56-8

5-(6-methoxynaphthalen-2-yl)-1H-pyrazole

3-(6-Methoxy-2-naphthyl)-1H-pyrazole

Ref: 54-OR111017