2-(5-(3,4-Dimethoxyphenyl)-1H-pyrazol-3-yl)naphthalen-1-ol, with the CAS number 371213-22-8, is a chemical compound characterized by its complex structure, which includes a naphthalene moiety and a pyrazole ring substituted with a dimethoxyphenyl group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as potential fluorescence and varied solubility in organic solvents. The presence of the hydroxyl group (naphthalen-1-ol) suggests it may engage in hydrogen bonding, influencing its solubility and reactivity. The dimethoxy groups can enhance the compound's lipophilicity and may also affect its biological activity, making it of interest in medicinal chemistry. Additionally, the pyrazole ring is known for its diverse pharmacological properties, including anti-inflammatory and analgesic effects. Overall, this compound's unique structural features may contribute to its potential applications in drug development and material science, although specific biological activities would require further investigation.

2-(5-(3,4-dimethoxyphenyl)-1H-pyrazol-3-yl)naphthalen-1-ol

371213-22-8: 2-(5-(3,4-Dimethoxyphenyl)-1H-pyrazol-3-yl)naphthalen-1-ol, with the CAS number 371213-22-8, is a chemical compound characterized by its complex structure, which includes a naphthalene moiety and a pyrazole ring substituted with a dimethoxyphenyl group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as potential fluorescence and varied solubility in organic solvents. The presence of the hydroxyl group (naphthalen-1-ol) suggests it may engage in hydrogen bonding, influencing its solubility and reactivity. The dimethoxy groups can enhance the compound's lipophilicity and may also affect its biological activity, making it of interest in medicinal chemistry. Additionally, the pyrazole ring is known for its diverse pharmacological properties, including anti-inflammatory and analgesic effects. Overall, this compound's unique structural features may contribute to its potential applications in drug development and material science, although specific biological activities would require further investigation.

<p>VEGFR-2-IN-65 (Compound 07) functions as a VEGFR-2 inhibitor. It forms hydrogen bonds with Cys180 and can inhibit tube formation in HUVECs.</p>

CAS 371213-22-8

2-(5-(3,4-dimethoxyphenyl)-1H-pyrazol-3-yl)naphthalen-1-ol

VEGFR-2-IN-65

Ref: TM-T205402