3-(Tert-butyl)-4-((4-((4-nitrophenyl)methoxy)phenyl)methylene)-1-phenyl-2-pyrazolin-5-one is a complex organic compound characterized by its pyrazolone core, which is a five-membered ring containing two nitrogen atoms. The presence of a tert-butyl group enhances its hydrophobic properties, potentially influencing its solubility and reactivity. The compound features a methylene bridge connecting a phenyl group to a 4-nitrophenyl moiety, which introduces electron-withdrawing characteristics due to the nitro group, likely affecting the compound's electronic properties and reactivity. The methoxy group contributes to the overall polarity and can participate in hydrogen bonding. This compound may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Its structural complexity suggests potential applications in pharmaceuticals or as a synthetic intermediate. However, specific properties such as melting point, boiling point, and spectral data would require experimental determination or literature reference for precise characterization.

3-(TERT-BUTYL)-4-((4-((4-NITROPHENYL)METHOXY)PHENYL)METHYLENE)-1-PHENYL-2-PYRAZOLIN-5-ONE

1024693-74-0: 3-(Tert-butyl)-4-((4-((4-nitrophenyl)methoxy)phenyl)methylene)-1-phenyl-2-pyrazolin-5-one is a complex organic compound characterized by its pyrazolone core, which is a five-membered ring containing two nitrogen atoms. The presence of a tert-butyl group enhances its hydrophobic properties, potentially influencing its solubility and reactivity. The compound features a methylene bridge connecting a phenyl group to a 4-nitrophenyl moiety, which introduces electron-withdrawing characteristics due to the nitro group, likely affecting the compound's electronic properties and reactivity. The methoxy group contributes to the overall polarity and can participate in hydrogen bonding. This compound may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Its structural complexity suggests potential applications in pharmaceuticals or as a synthetic intermediate. However, specific properties such as melting point, boiling point, and spectral data would require experimental determination or literature reference for precise characterization.

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CAS 1024693-74-0

3-(TERT-BUTYL)-4-((4-((4-NITROPHENYL)METHOXY)PHENYL)METHYLENE)-1-PHENYL-2-PYRAZOLIN-5-ONE

3-(tert-butyl)-4-((4-((4-nitrophenyl)methoxy)phenyl)methylene)-1-phenyl-2-pyrazolin-5-one

Ref: 3D-ZQB69374