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Structure of 315188-30-8
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2-Amino-5-bromo-4-fluorobenzaldehyde features a trifunctional aromatic core with electron-donating amino and halogen substituents that enable selective coupling in pharmaceutical synthesis. The aldehyde group provides a handle for nucleophilic addition, while the bromo and fluoro moieties facilitate palladium-catalyzed cross-coupling reactions. This compound serves as a key intermediate in the construction of bioactive heterocycles and functionalized aryl scaffolds under standard conditions.
2-Amino-5-bromo-4-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted heterocycles and bioactive scaffolds. Its orthogonal functional groups—amine, bromo, fluoro, and aldehyde—facilitate diverse downstream transformations including Suzuki-Miyaura coupling, nucleophilic substitution, and condensation reactions. The compound exhibits good bench stability and is amenable to standard purification methods, making it well-suited for scalable synthesis and target-oriented drug discovery campaigns.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: