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Structure of 34784-02-6
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3-Bromoisoquinoline features a bromine substituent at the 3-position of the isoquinoline core, enabling direct functionalization in cross-coupling reactions. This electron-deficient heterocycle serves as a key intermediate in medicinal chemistry and materials synthesis, offering high reactivity and compatibility with palladium-catalyzed transformations under standard conditions.
3-Bromoisoquinoline serves as a versatile building block in medicinal chemistry and catalytic synthesis, enabling palladium-catalyzed cross-coupling reactions such as Suzuki, Stille, and Negishi transformations. Its well-established reactivity facilitates the construction of biaryl and heteroaryl scaffolds common in pharmaceuticals. The bromine substituent provides excellent functional group tolerance and bench stability, simplifying purification and handling in multi-step syntheses.
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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: