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Structure of 891180-59-9
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2-Bromo-3-fluorobenzaldehyde features a fluorine atom adjacent to a bromine-substituted aromatic ring, enabling selective functionalization in cross-coupling reactions. The aldehyde group provides a reactive handle for nucleophilic additions and condensation chemistry. This electron-deficient aryl aldehyde exhibits enhanced stability under standard conditions and facilitates the synthesis of complex heterocycles and pharmaceutical intermediates.
2-Bromo-3-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct incorporation of halogenated aromatic motifs. Its ortho-halogenated benzaldehyde framework facilitates palladium-catalyzed cross-coupling reactions and supports further functionalization via electrophilic substitution or nucleophilic addition. The molecule exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthetic sequences and scale-up 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: