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Structure of 885952-16-9
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2,3-Dibromo-6-chloropyridine features a halogenated pyridine core with complementary reactivity at multiple positions. The electron-deficient aromatic ring enables efficient cross-coupling transformations, while the bromine and chlorine substituents offer orthogonal functionalization pathways. This bench-stable compound integrates readily into complex heterocyclic scaffolds under standard conditions.
2,3-Dibromo-6-chloropyridine serves as a versatile building block in heterocyclic synthesis, enabling regioselective functionalization at the 2- and 3-positions via palladium-catalyzed cross-coupling reactions. The presence of two bromine atoms and a chlorine substituent provides orthogonal reactivity for sequential transformations, facilitating access to complex pyridine-based scaffolds. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-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: