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Structure of 116986-13-1
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3-(Bromomethyl)picolinonitrile features a bromomethyl group attached to the pyridine ring, enabling efficient nucleophilic substitution reactions. The nitrile moiety provides strong electron-withdrawing character, enhancing reactivity at the benzylic position. This compound serves as a key building block for heterocyclic synthesis and functionalized intermediates in medicinal chemistry.
3-(Bromomethyl)picolinonitrile serves as a versatile bifunctional building block for medicinal and synthetic chemistry, enabling efficient construction of heterocyclic scaffolds. The bromomethyl group facilitates nucleophilic substitution reactions, while the picolinonitrile moiety provides a polar, electron-deficient site compatible with transition-metal-catalyzed couplings. Its bench-stable nature and compatibility with diverse functional groups make it ideal for iterative synthesis workflows in API development and library generation.
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GHS No : GHS06
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Signal Word : Danger
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UN#: 3439
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302+H312-H315-H319-H331-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: