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Structure of 168015-04-1
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2-Bromo-6-(hydroxymethyl)pyridin-3-ol features a pyridine core bearing a bromo group at the 2-position and a hydroxymethyl function at the 6-position, flanked by a phenolic hydroxyl at the 3-position. This trifunctional scaffold enables direct incorporation into heterocyclic architectures via cross-coupling or cyclization reactions under standard conditions. The molecule exhibits enhanced solubility in polar solvents and maintains stability during storage.
2-Bromo-6-(hydroxymethyl)pyridin-3-ol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyridine-based scaffolds through palladium-catalyzed coupling reactions. The pendant hydroxymethyl group offers orthogonal reactivity for derivatization, while the bromide facilitates cross-coupling under standard conditions. Bench-stable and compatible with common purification methods, it supports scalable workflows in medicinal chemistry and materials science applications.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: