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Structure of 1258287-39-6
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5-Bromo-2-methylpyridin-4-ol features a bromine substituent at the 5-position and a methyl group at the 2-position, flanking a phenolic hydroxyl at the 4-position. This arrangement imparts enhanced reactivity in cross-coupling processes, enabling efficient incorporation into complex heterocyclic scaffolds under mild conditions. The molecule exhibits robust stability and solubility in polar aprotic solvents, facilitating use in synthetic workflows requiring precise functionalization.
5-Bromo-2-methylpyridin-4-ol serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling direct functionalization via palladium-catalyzed cross-coupling reactions. The bromo group at the 5-position provides high reactivity in Suzuki, Stille, and Negishi couplings, while the hydroxyl and methyl groups offer orthogonal handles for further derivatization. Its bench-stable solid form facilitates handling and purification, making it ideal for scalable synthesis of pyridine-based pharmaceutical intermediates and agrochemical scaffolds.
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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: