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Structure of 1196152-02-9
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4-Bromo-2-chloro-6-methoxypyridine features a pyridine core functionalized with bromo, chloro, and methoxy groups at the 4, 2, and 6 positions, respectively. This electron-deficient heterocycle enables selective cross-coupling reactions under palladium catalysis, serving as a key building block in pharmaceutical synthesis. The methoxy group enhances solubility and modulates reactivity.
4-Bromo-2-chloro-6-methoxypyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo group facilitates Suzuki, Stille, or Negishi couplings, while the chloro and methoxy substituents provide directional control and enhanced stability. This compound exhibits excellent bench stability and is readily purified by chromatography, making it ideal for iterative synthesis of complex 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+H312+H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: