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Structure of 778611-64-6
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5-Bromo-2-chloro-4-methylpyridine features a tri-substituted pyridine core with distinct halogen and methyl functionalities. The bromo group at C5 enables facile cross-coupling, while the chloro moiety at C2 offers complementary reactivity. This electronic and steric profile supports efficient incorporation into complex heterocyclic architectures under standard conditions.
5-Bromo-2-chloro-4-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The bromo group facilitates efficient Suzuki, Stille, or Negishi coupling, while the chloro and methyl functionalities provide orthogonal functionalization potential. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for constructing complex heterocyclic scaffolds in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: