3-Biphenyl-4-yl-1-phenyl-1H-pyrazole-4-carbaldehyde, with the CAS number 108446-64-6, is an organic compound characterized by its complex structure, which includes a pyrazole ring and multiple aromatic systems. This compound typically exhibits properties associated with both aldehydes and pyrazoles, such as reactivity towards nucleophiles due to the presence of the aldehyde functional group. It may display significant fluorescence or photochemical properties, making it of interest in various applications, including organic synthesis and materials science. The presence of biphenyl and phenyl groups contributes to its hydrophobic nature and potential for π-π stacking interactions, which can influence its solubility and stability in different solvents. Additionally, the compound may exhibit biological activity, making it a candidate for further research in medicinal chemistry. Its synthesis and characterization would typically involve standard organic reactions, and its purity and identity can be confirmed through techniques such as NMR spectroscopy and mass spectrometry.

3-BIPHENYL-4-YL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE

108446-64-6: 3-Biphenyl-4-yl-1-phenyl-1H-pyrazole-4-carbaldehyde, with the CAS number 108446-64-6, is an organic compound characterized by its complex structure, which includes a pyrazole ring and multiple aromatic systems. This compound typically exhibits properties associated with both aldehydes and pyrazoles, such as reactivity towards nucleophiles due to the presence of the aldehyde functional group. It may display significant fluorescence or photochemical properties, making it of interest in various applications, including organic synthesis and materials science. The presence of biphenyl and phenyl groups contributes to its hydrophobic nature and potential for π-π stacking interactions, which can influence its solubility and stability in different solvents. Additionally, the compound may exhibit biological activity, making it a candidate for further research in medicinal chemistry. Its synthesis and characterization would typically involve standard organic reactions, and its purity and identity can be confirmed through techniques such as NMR spectroscopy and mass spectrometry.

CAS 108446-64-6

3-BIPHENYL-4-YL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE

1-Phenyl-3-(4-phenylphenyl)-1H-pyrazole-4-carbaldehyde

Ref: 3D-IEA44664