9H-Xanthen-9-one, 2,7-dibromo- is an organic compound characterized by its xanthone structure, which consists of a fused benzopyranone system. This compound features two bromine substituents at the 2 and 7 positions of the xanthone core, which can significantly influence its chemical properties and reactivity. Typically, xanthones exhibit fluorescence and are known for their potential biological activities, including antimicrobial and antioxidant properties. The presence of bromine atoms can enhance the compound's lipophilicity and may affect its interaction with biological targets. In terms of physical properties, xanthones generally have moderate solubility in organic solvents and limited solubility in water. The compound's molecular structure contributes to its stability, although the bromine substituents may introduce some reactivity under certain conditions. Overall, 9H-Xanthen-9-one, 2,7-dibromo- is of interest in various fields, including organic synthesis, materials science, and medicinal chemistry, due to its unique structural features and potential applications.

9H-Xanthen-9-one, 2,7-dibromo-

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