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Structure of 1206968-77-5
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2-(5-Bromopyridin-2-yl)ethanol features a brominated pyridine ring linked via an ethylene tether, enabling direct incorporation into cross-coupling and functionalization workflows. The pendant hydroxyl group offers a handle for derivatization, while the electron-deficient heterocycle enhances reactivity in palladium-catalyzed transformations. This bench-stable reagent integrates efficiently into synthetic sequences requiring halogenated aromatic motifs.
2-(5-Bromopyridin-yl)ethanol serves as a versatile building block in medicinal chemistry, enabling direct functionalization of pyridine cores via nucleophilic substitution or cross-coupling reactions. Its bromo group facilitates Pd-catalyzed transformations, while the terminal hydroxyl group offers straightforward derivatization for conjugation or protection. The molecule exhibits good bench stability and is compatible with standard purification protocols, making it a reliable reagent for constructing complex 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-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: