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Structure of 144873-99-4
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2-(6-Bromopyridin-3-yl)acetonitrile features a brominated pyridine ring paired with a nitrile-bearing side chain, enabling direct coupling in cross-coupling reactions. This bench-stable reagent integrates readily into synthetic sequences requiring halogen-directed functionalization, offering high compatibility with palladium catalysis and efficient access to complex heterocyclic architectures.
2-(6-Bromopyridin-3-yl)acetonitrile serves as a versatile building block in cross-coupling reactions, enabling efficient access to substituted pyridine scaffolds. The bromine and nitrile groups provide orthogonal reactivity for palladium-catalyzed coupling and nucleophilic transformations, respectively. Its bench-stable nature and compatibility with standard purification methods make it well-suited for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2923
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Class : 8(6.1)
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H318-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: