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Structure of 18014-00-1
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Dimethyl 2,5-dibromoterephthalate features a rigid aromatic core with bromine substituents at the para positions, enabling high reactivity in cross-coupling processes. The dimethyl ester groups facilitate smooth functionalization under standard conditions. This bench-stable compound integrates readily into modular synthetic sequences for advanced materials and pharmaceutical intermediates.
Dimethyl 2,5-dibromoterephthalate serves as a versatile dihalogenated building block for the synthesis of functionalized aromatic scaffolds. Its bromine substituents enable palladium-catalyzed cross-coupling reactions, facilitating the construction of biaryl and polyaromatic systems. The dimethyl ester groups offer compatibility with standard hydrolysis and derivatization protocols, supporting downstream modifications in pharmaceutical and materials chemistry workflows.
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Lot numbers can be found on the outside label of a product: