3,5,7,8-Tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one, also known as $name$, is a versatile compound utilized in chemical synthesis for its unique structural properties and reactivity. In the field of organic chemistry, $name$ serves as a key building block for the synthesis of various bioactive compounds, pharmaceuticals, and natural products. Its hydroxyl groups at positions 3, 5, 7, and 8 make it an ideal candidate for molecular modifications and derivatization, allowing for the creation of new molecules with desirable properties. Additionally, the presence of a phenolic group at position 4 enables $name$ to participate in diverse chemical reactions, such as O-alkylation, O-acylation, and oxidative transformations, further expanding its synthetic utility.In chemical synthesis, 3,5,7,8-Tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one is commonly employed as a scaffold for the construction of polyphenolic compounds with antioxidant, antimicrobial, and anti-inflammatory activities. By functionalizing different positions of the chromenone core, chemists can fine-tune the biological properties of the resulting molecules, making $name$ a valuable tool in drug discovery and development. Moreover, the regioselective nature of $name$ allows for precise manipulation of its structure, facilitating the synthesis of complex molecules with high purity and yield. Overall, the versatility and reactivity of 3,5,7,8-Tetrahydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one make it a valuable asset in the toolbox of synthetic chemists seeking to access novel compounds with therapeutic potential.
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