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Structure of 5629-98-1
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2,4-Dibromobenzaldehyde features two bromine substituents at the 2- and 4-positions of the benzene ring, delivering enhanced electrophilicity at the carbonyl center. This electron-deficient aldehyde integrates readily into cross-coupling reactions and serves as a robust building block for functionalized aromatic scaffolds in medicinal chemistry and materials synthesis.
2,4-Dibromobenzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to brominated aromatic scaffolds via cross-coupling and electrophilic substitution reactions. Its dual bromine substituents provide orthogonal reactivity for sequential functionalization, while the aldehyde group facilitates condensation, reduction, or imine formation. Bench-stable and readily purified by recrystallization, it functions reliably in the synthesis of pharmaceutical intermediates and functionalized heterocycles.
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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: