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Structure of 22532-61-2
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2-Bromo-6-hydroxybenzaldehyde features a bromine atom at the ortho position relative to the aldehyde, paired with a hydroxyl group at the para position, creating a uniquely activated aromatic scaffold. This combination enables direct functionalization in cross-coupling and oxidation reactions, while the phenolic OH enhances solubility and facilitates chelation in catalytic systems. The molecule exhibits robust stability under standard bench conditions, allowing straightforward handling in synthetic workflows.
2-Bromo-6-hydroxybenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the aromatic ring and aldehyde site. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the hydroxyl and aldehyde functionalities offer orthogonal handles for derivatization. The compound exhibits good bench stability and is compatible with standard protecting group strategies, making it valuable for constructing complex heterocyclic scaffolds and pharmaceutical intermediates.
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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: