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Structure of 22532-60-1
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2-Bromo-4-hydroxybenzaldehyde features a bromine atom at the ortho position relative to the aldehyde, combined with a para-hydroxyl group that imparts enhanced polarity and hydrogen-bonding capacity. This electronic configuration supports its use in coupling reactions and as a building block for bioactive heterocycles. The compound exhibits good stability under standard bench conditions and facilitates efficient functionalization in synthetic pathways.
2-Bromo-4-hydroxybenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the phenolic hydroxyl and aldehyde positions. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the aldehyde group supports reductive amination and condensation protocols. The compound exhibits good bench stability and is readily purified by crystallization, making it well-suited for multi-step synthetic sequences requiring orthogonal reactivity.
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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: