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Structure of 1256823-65-0
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5-Bromo-6-chloropicolinonitrile features a highly functionalized pyridine core with orthogonal halogen and nitrile groups, enabling selective coupling in cross-coupling reactions. The electron-deficient ring facilitates nucleophilic substitution, while the steric profile supports controlled reaction pathways. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and advanced pharmaceuticals.
5-Bromo-6-chloropicolinonitrile serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen functionality. The nitrile group provides a handle for selective transformations, while the bromo and chloro substituents offer complementary reactivity for sequential functionalization. Bench-stable and amenable to purification by recrystallization, it facilitates efficient access to substituted pyridine scaffolds relevant to medicinal chemistry and agrochemical development.
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GHS Pictogram :
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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: