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Structure of 1211584-86-9
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6-Bromo-4-chloropyridin-3-ol features a pyridinol core with bromo and chloro substituents at the 6- and 4-positions, respectively, enabling selective functionalization in medicinal chemistry. The hydroxyl group enhances solubility and serves as a handle for derivatization. This compound is bench-stable and compatible with standard cross-coupling protocols.
6-Bromo-4-chloropyridin-3-ol serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen functionality. The bromo group facilitates Suzuki, Stille, or Negishi coupling, while the chloro and hydroxyl groups offer complementary reactivity for further derivatization. Its bench-stable nature and compatibility with standard purification methods support efficient 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: