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Structure of 23003-29-4
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2,4-Dibromo-6-methylpyridin-3-ol features a pyridinol core with bromine substituents at the 2 and 4 positions and a methyl group at the 6 position, creating a sterically hindered, electron-deficient heterocyclic scaffold. This configuration enables direct coupling in cross-coupling reactions and facilitates functionalization in medicinal chemistry applications.
2,4-Dibromo-6-methylpyridin-3-ol serves as a versatile building block in heterocyclic synthesis, enabling efficient Suzuki-Miyaura and Buchwald-Hartwig coupling reactions. The bromine atoms exhibit high reactivity under palladium catalysis, while the phenolic hydroxyl group provides orthogonal functionality for derivatization. Bench-stable and readily purified by recrystallization, it functions effectively in the construction of substituted pyridine scaffolds relevant to medicinal chemistry and agrochemical development.
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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: