The chemical substance known as 3-(2-(3-chloro-5-(trifluoromethyl)(2-pyridyloxy))phenyl)-1-phenylprop-2-en-1-one, with the CAS number 1025643-55-3, is a complex organic compound characterized by its unique structural features. It contains multiple functional groups, including a phenylprop-2-en-1-one moiety, which suggests it may exhibit properties typical of chalcones, such as potential biological activity. The presence of a trifluoromethyl group and a chloro substituent indicates that the compound may possess significant lipophilicity and could interact with biological targets, making it of interest in medicinal chemistry. Additionally, the pyridyloxy group may contribute to its solubility and reactivity. The compound's molecular structure suggests it may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-withdrawing effects of the halogen and trifluoromethyl groups. Overall, this compound's unique characteristics may provide insights into its potential applications in pharmaceuticals or agrochemicals, although specific biological activity would require further investigation.

3-(2-(3-CHLORO-5-(TRIFLUOROMETHYL)(2-PYRIDYLOXY))PHENYL)-1-PHENYLPROP-2-EN-1-ONE

1025643-55-3: The chemical substance known as 3-(2-(3-chloro-5-(trifluoromethyl)(2-pyridyloxy))phenyl)-1-phenylprop-2-en-1-one, with the CAS number 1025643-55-3, is a complex organic compound characterized by its unique structural features. It contains multiple functional groups, including a phenylprop-2-en-1-one moiety, which suggests it may exhibit properties typical of chalcones, such as potential biological activity. The presence of a trifluoromethyl group and a chloro substituent indicates that the compound may possess significant lipophilicity and could interact with biological targets, making it of interest in medicinal chemistry. Additionally, the pyridyloxy group may contribute to its solubility and reactivity. The compound's molecular structure suggests it may participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks, due to the electron-withdrawing effects of the halogen and trifluoromethyl groups. Overall, this compound's unique characteristics may provide insights into its potential applications in pharmaceuticals or agrochemicals, although specific biological activity would require further investigation.

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CAS 1025643-55-3

3-(2-(3-CHLORO-5-(TRIFLUOROMETHYL)(2-PYRIDYLOXY))PHENYL)-1-PHENYLPROP-2-EN-1-ONE

3-(2-(3-chloro-5-(trifluoromethyl)(2-pyridyloxy))phenyl)-1-phenylprop-2-en-1-one

Ref: 3D-ARB64355