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Structure of 1005291-43-9
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2-Bromo-5-fluoroisonicotinaldehyde delivers a strategically positioned bromo and fluoro substitution on an isonicotinaldehyde scaffold, enabling direct incorporation into cross-coupling reactions and heterocyclic syntheses. The aldehyde functionality offers high reactivity under mild conditions, while the electron-deficient pyridine ring enhances regioselectivity in transition-metal-catalyzed transformations.
2-Bromo-5-fluoroisonicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogenation pattern. The aldehyde functionality facilitates direct derivatization via reductive amination or nucleophilic addition, while the fluorine and bromine substituents offer tunable electronic effects and compatibility with standard heterocycle synthesis protocols. Its bench-stable nature and ease of purification support efficient workflow integration in API and fragment-based discovery programs.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: