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Structure of 77771-02-9
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3-Bromo-4-fluorobenzaldehyde features a strategically positioned bromine and fluorine substituent on the benzene ring, enabling selective cross-coupling reactions. The aldehyde functionality provides a direct handle for nucleophilic addition or condensation processes. This electron-deficient aromatic scaffold offers enhanced reactivity in palladium-catalyzed transformations and is compatible with standard bench protocols.
3-Bromo-4-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The aldehyde group facilitates direct functionalization or condensation reactions, while the bromo and fluoro substituents provide excellent compatibility with standard transition-metal catalysis and enhanced metabolic stability in bioactive scaffolds. Bench-stable and readily purified by distillation, it functions reliably in multi-step syntheses.
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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: