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Structure of 13985-15-4
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2,3,6,7-Tetramethoxy-9,10-dimethylanthracene features a rigid polycyclic core with four methoxy groups enhancing solubility and electron-donating capacity, while the methyl substituents at positions 9 and 10 stabilize the excited state. This configuration enables efficient charge transfer in donor-acceptor systems, making it valuable for organic optoelectronic applications.
2,3,6,7-Tetramethoxy-9,10-dimethylanthracene serves as a robust polycyclic scaffold for organic synthesis, offering enhanced solubility and stability due to its methoxy and methyl substituents. The anthracene core enables reliable Diels-Alder reactivity and functions as a building block in the construction of functionalized heterocycles and advanced materials. Its bench-stable nature and predictable regiochemistry facilitate straightforward purification and integration into multi-step synthetic sequences.
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Lot numbers can be found on the outside label of a product: