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Structure of 7321-27-9
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2-Bromoanthracene features a bromine atom positioned at the 2-adjacent site of the anthracene core, creating a highly reactive electrophilic center. This strategic substitution enables direct integration into palladium-catalyzed cross-coupling reactions, delivering functionalized polycyclic architectures with high regiocontrol. The compound exhibits excellent stability under standard bench conditions and serves as a key intermediate in synthetic pathways targeting advanced organic materials and pharmaceutical candidates.
2-Bromoanthracene serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions such as Suzuki, Stille, and Negishi couplings. Its anthracene core provides enhanced planarity and electronic delocalization, facilitating efficient π–π stacking in materials applications. The bromine substituent offers high reactivity under standard catalytic conditions with excellent functional group tolerance, making it ideal for constructing complex polycyclic architectures and advanced organic semiconductors.
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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: