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Structure of 109179-31-9
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2-Bromo-3-methylbenzaldehyde features a strategically positioned bromine atom and methyl group on the aromatic ring, enabling selective functionalization in cross-coupling reactions. This electron-deficient aldehyde integrates readily into complex molecular architectures under standard conditions.
2-Bromo-3-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct incorporation of bromo and methyl substituents adjacent to an aldehyde handle. Its reactivity facilitates palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Stille couplings, with excellent functional group tolerance. The aldehyde group supports subsequent transformations such as imine formation, oxime derivatization, or reductive amination, while the molecule exhibits good bench stability and ease of purification, making it well-suited for iterative synthetic sequences and scale-up.
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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: