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Structure of 31558-41-5
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4-Bromo-2,5-dimethoxybenzaldehyde features a bromine substituent at the para position relative to the aldehyde, flanked by two methoxy groups that enhance electron density. This combination enables selective coupling reactions in synthetic routes to bioactive compounds. The molecule exhibits bench-stable handling characteristics and compatibility with standard reaction conditions in medicinal chemistry workflows.
4-Bromo-2,5-dimethoxybenzaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the two methoxy groups provide orthogonally protected phenolic sites. The aldehyde functionality facilitates condensation reactions and imine formation, supporting rapid access to diverse scaffolds. Bench-stable and amenable to standard purification methods, it functions effectively in multi-step syntheses requiring functional group compatibility and predictable 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: