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Structure of 63525-48-4
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2,5-Dibromoterephthalaldehyde features two bromine atoms positioned at the para and meta sites relative to the aldehyde groups, creating a highly functionalized aromatic scaffold. This electron-deficient core enables selective coupling reactions in synthetic organic chemistry, particularly in cross-coupling and cyclization processes. The molecule exhibits enhanced stability under standard bench conditions and integrates readily into complex molecular architectures requiring halogen-directed functionalization.
2,5-Dibromoterephthalaldehyde serves as a versatile dihalogenated aromatic aldehyde building block for the synthesis of functionalized heterocycles and conjugated materials. Its orthogonal reactivity—enabling selective cross-coupling, nucleophilic addition, or oxidative transformations—makes it valuable in medicinal chemistry and materials science applications. Bench-stable and readily purified by recrystallization, it functions effectively in Pd-catalyzed coupling protocols and serves as a key intermediate in the construction of complex aromatic scaffolds.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: