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Structure of 318276-72-1
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6-Bromocinnoline features a bromine substituent at the 6-position of the cinnoline core, enabling direct functionalization in transition-metal-catalyzed coupling reactions. This electron-deficient heterocycle integrates readily into pharmaceutical and agrochemical scaffolds, offering enhanced reactivity in cross-coupling processes under standard conditions.
6-Bromocinnoline serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions to construct biaryl and heteroaryl scaffolds. Its bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the cinnoline core offers inherent stability and compatibility with diverse functional groups. This compound facilitates efficient access to nitrogen-containing heterocycles relevant in medicinal chemistry and materials science, with excellent bench stability and straightforward purification.
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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: