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Structure of 1256822-16-8
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2-Bromo-5-fluoroisonicotinonitrile features a strategically positioned bromine and fluorine substituent on the pyridine ring, enabling selective cross-coupling reactions. The nitrile group provides a handle for downstream functionalization, while the electron-deficient core enhances reactivity in palladium-catalyzed transformations under standard conditions.
2-Bromo-5-fluoroisonicotinonitrile serves as a versatile building block in medicinal chemistry, enabling late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its orthogonal reactivity profile—combining a nitrile group for downstream transformations and halogenation sites for selective derivatization—facilitates efficient access to substituted heterocycles and API scaffolds. The compound exhibits good bench stability and is compatible with standard synthetic workflows.
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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-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: