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Structure of 199177-26-9
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3-Bromo-5-hydroxybenzaldehyde features a bromine substituent and a hydroxyl group flanking the aldehyde functionality, enabling selective coupling reactions. This electron-deficient aromatic scaffold supports efficient derivatization in synthetic medicinal chemistry workflows.
3-Bromo-5-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry, enabling direct functionalization at both the hydroxyl and aldehyde positions. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the phenolic hydroxyl allows for derivatization or protection. The aldehyde functionality supports reductive amination, Mannich reactions, and imine formation, making it valuable for constructing heterocyclic scaffolds and bioactive intermediates. Bench-stable and compatible with standard purification methods, it functions reliably in multi-step synthesis workflows.
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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: