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Structure of 1211523-71-5
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2-(2-Bromopyridin-3-yl)acetonitrile features a brominated pyridine ring paired with a nitrile-bearing acetyl side chain, enabling direct incorporation into cross-coupling and cyclization workflows. The electron-deficient heteroaryl moiety facilitates palladium-catalyzed transformations, while the nitrile group serves as a handle for downstream functionalization. This compound offers high reactivity under standard conditions with excellent bench stability.
2-(2-Bromopyridin-3-yl)acetonitrile serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of biologically relevant heterocyclic scaffolds. The bromine and nitrile functionalities provide orthogonal reactivity for palladium-catalyzed cross-coupling and nucleophilic transformations, respectively. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for iterative synthesis in medicinal chemistry and process development 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-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: