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Structure of 1370411-47-4
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3-Bromo-5-fluoro-4-methylbenzaldehyde features a trifunctional aromatic core with bromo, fluoro, and methyl substituents positioned for orthogonal reactivity. The aldehyde group enables direct coupling in cross-coupling or condensation reactions. This electron-deficient aryl scaffold offers enhanced stability under standard conditions and facilitates selective functionalization in synthetic sequences.
3-Bromo-5-fluoro-4-methylbenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of complex heterocyclic scaffolds. Its ortho-halogenated aryl core facilitates palladium-catalyzed cross-coupling reactions, while the aldehyde functionality supports reductive amination, Schiff base formation, and oxime derivatization. The methyl group provides a site for oxidation or functionalization, and the molecule exhibits good bench stability and compatibility with standard purification methods.
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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: