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Structure of 26254-35-3
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5-Bromoacenaphthenequinone features a bromine substituent at the 5-position of the acenaphthenequinone scaffold, enhancing its reactivity in cross-coupling processes. This electron-deficient quinone integrates readily into synthetic pathways requiring halogenated aromatic intermediates. The molecule exhibits bench-stable handling characteristics and maintains structural integrity under standard reaction conditions.
5-Bromoacenaphthenequinone serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine functionality. The acenaphthenequinone core provides a rigid, electron-deficient aromatic system that facilitates Diels-Alder cycloadditions and nucleophilic substitutions. Its bench-stable crystalline form simplifies handling and purification, making it suitable for iterative synthesis of complex polycyclic scaffolds and functionalized heterocycles in medicinal chemistry and materials science applications.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: