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Structure of 40273-45-8
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2-Bromo-3-fluoropyridine features a fluorine atom at the 3-position and bromine at the 2-position of the pyridine ring, creating a strategically positioned halogen pair. This arrangement enables selective cross-coupling reactions in transition-metal catalysis, particularly in Suzuki-Miyaura and Negishi transformations. The electron-deficient nature of the ring enhances reactivity in nucleophilic substitution pathways. Bench-stable under standard conditions, it serves as a key building block for pharmaceutical intermediates and functionalized heterocycles.
2-Bromo-3-fluoropyridine 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 bromo group facilitates efficient C–C bond formation, while the fluorine substituent enhances metabolic stability and modulates electronic properties. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds in drug discovery workflows.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H315-H319
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: