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Structure of 1256833-80-3
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2-Bromo-6-chloronicotinonitrile features a highly functionalized pyridine core bearing bromo, chloro, and nitrile groups at the 2-, 6-, and 3-positions, respectively. This electron-deficient heterocycle serves as a key building block in agrochemical and pharmaceutical synthesis, enabling efficient coupling reactions under standard conditions. The strategic placement of halogens facilitates selective cross-coupling transformations, while the nitrile group offers additional anchoring points for derivatization.
2-Bromo-6-chloronicotinonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The nitrile group provides a handle for further functionalization, while the ortho-bromo and meta-chloro substituents offer orthogonal reactivity for sequential transformations. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthesis of heterocyclic scaffolds and API intermediates.
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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: