3-(Tert-butyl)-1-(5-(trifluoromethyl)(2-pyridyl))indeno[2,3-d]pyrazol-4-one is a complex organic compound characterized by its unique structural features, including an indeno[2,3-d]pyrazol core, a tert-butyl group, and a trifluoromethyl-substituted pyridine moiety. This compound typically exhibits properties such as moderate to high lipophilicity due to the presence of the tert-butyl group, which can influence its solubility in organic solvents. The trifluoromethyl group is known for enhancing the compound's biological activity and stability, while the pyridine ring can participate in various chemical interactions, including hydrogen bonding and coordination with metal ions. The presence of the pyrazolone functional group suggests potential reactivity, particularly in forming derivatives through nucleophilic substitution or condensation reactions. Overall, this compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential biological activity and structural diversity. However, specific properties such as melting point, boiling point, and spectral data would require experimental determination or detailed literature references for precise characterization.

3-(TERT-BUTYL)-1-(5-(TRIFLUOROMETHYL)(2-PYRIDYL))INDENO[2,3-D]PYRAZOL-4-ONE

1024537-54-9: 3-(Tert-butyl)-1-(5-(trifluoromethyl)(2-pyridyl))indeno[2,3-d]pyrazol-4-one is a complex organic compound characterized by its unique structural features, including an indeno[2,3-d]pyrazol core, a tert-butyl group, and a trifluoromethyl-substituted pyridine moiety. This compound typically exhibits properties such as moderate to high lipophilicity due to the presence of the tert-butyl group, which can influence its solubility in organic solvents. The trifluoromethyl group is known for enhancing the compound's biological activity and stability, while the pyridine ring can participate in various chemical interactions, including hydrogen bonding and coordination with metal ions. The presence of the pyrazolone functional group suggests potential reactivity, particularly in forming derivatives through nucleophilic substitution or condensation reactions. Overall, this compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential biological activity and structural diversity. However, specific properties such as melting point, boiling point, and spectral data would require experimental determination or detailed literature references for precise characterization.

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CAS 1024537-54-9

3-(TERT-BUTYL)-1-(5-(TRIFLUOROMETHYL)(2-PYRIDYL))INDENO[2,3-D]PYRAZOL-4-ONE

3-(tert-butyl)-1-(5-(trifluoromethyl)(2-pyridyl))indeno[2,3-d]pyrazol-4-one

Ref: 3D-ZQB53754