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Structure of 254744-15-5
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4-Bromo-3-(hydroxymethyl)benzaldehyde features a bromine substituent at the para position relative to the aldehyde, enhancing electrophilic reactivity. The adjacent hydroxymethyl group provides a handle for derivatization, while the aldehyde moiety enables direct incorporation into coupling reactions. This compound serves as a key intermediate in the synthesis of functionalized aromatic systems and bioactive molecules.
4-Bromo-3-(hydroxymethyl)benzaldehyde serves as a versatile building block in medicinal chemistry and materials synthesis, enabling efficient access to functionalized aromatic scaffolds. The aldehyde group facilitates nucleophilic additions and condensation reactions, while the bromide supports palladium-catalyzed cross-couplings. The hydroxymethyl functionality offers additional handles for derivatization or protection, enhancing synthetic flexibility. Its bench-stable nature and compatibility with common reaction conditions make it a practical choice for multi-step syntheses.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: