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Structure of 351457-86-8
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5-Bromo-4-methylnicotinaldehyde delivers a reactive aldehyde group flanked by a bromine atom and a methyl substituent on the pyridine ring. This electronic and steric configuration enables direct coupling in cross-coupling reactions, facilitating rapid access to functionalized heterocycles under standard conditions.
5-Bromo-4-methylnicotinaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted pyridine scaffolds via cross-coupling and condensation reactions. The aldehyde functionality facilitates direct functionalization or imine formation, while the bromo group supports palladium-catalyzed coupling processes. Bench-stable and compatible with diverse reaction conditions, it functions effectively in medicinal chemistry campaigns targeting heterocyclic lead compounds.
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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: