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Structure of 1334499-25-0
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Methyl 5-bromo-6-hydroxy-2-methylpyridine-3-carboxylate features a brominated pyridine core with orthogonal functional groups enabling direct derivatization. The hydroxy and ester moieties offer strategic handles for cross-coupling, cyclization, or bioconjugation under mild conditions. This bench-stable intermediate supports rapid access to substituted heterocycles in medicinal chemistry and agrochemical synthesis.
Methyl 5-bromo-6-hydroxy-2-methylpyridine-3-carboxylate serves as a versatile building block for pyridine-based heterocycles, enabling direct functionalization at C5 and C6 positions. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the hydroxyl function supports derivatization or protection strategies. Bench-stable and compatible with standard synthetic workflows, it functions effectively in the construction of medicinally relevant scaffolds through orthogonal reactivity.
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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: