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Structure of 22532-62-3
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4-Bromo-2-hydroxybenzaldehyde features a bromine substituent at the para position relative to the aldehyde, combined with a phenolic hydroxyl group ortho to the carbonyl. This arrangement imparts enhanced electron-withdrawing character and facilitates intramolecular hydrogen bonding, improving stability and directing electrophilic substitution reactions. The compound serves as a key intermediate in synthesizing bioactive heterocycles and functionalized aromatic scaffolds under standard conditions.
4-Bromo-2-hydroxybenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling direct access to substituted benzofurans and other heterocyclic scaffolds via electrophilic cyclization. The ortho-hydroxy aldehyde functionality facilitates efficient intramolecular reactions, while the bromine substituent provides a reliable handle for palladium-catalyzed cross-coupling transformations. Its bench-stable crystalline form and compatibility with standard purification methods make it well-suited for iterative synthesis workflows in medicinal chemistry and materials development.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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Signal Word : Warning
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UN#: 3077
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H302-H410
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Precautionary Statements : P264-P270-P273-P330-P391-P501
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Lot numbers can be found on the outside label of a product: