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Structure of 2973-59-3
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2-Bromo-5-hydroxy-4-methoxybenzaldehyde features a brominated aromatic core with complementary hydroxyl and methoxy substituents, enabling selective coupling in cross-coupling reactions. The aldehyde group provides a reactive handle for conjugation, while the electron-donating methoxy and hydroxyl groups enhance regioselectivity. This compound offers improved stability and solubility under standard bench conditions, facilitating efficient synthesis in medicinal chemistry workflows.
2-Bromo-5-hydroxy-4-methoxybenzaldehyde serves as a versatile building block in the synthesis of bioactive heterocycles and functionalized aromatic scaffolds. Its orthogonal functionality—bromine for cross-coupling, hydroxyl for derivatization, methoxy for electronic modulation, and aldehyde for condensation reactions—enables efficient access to complex molecular architectures. Bench-stable and compatible with standard reaction protocols, it facilitates rapid diversification in medicinal chemistry and materials science applications.
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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: