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Structure of 159533-68-3
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1-(5-Bromopyridin-2-yl)ethan-1-ol features a brominated pyridine ring linked to a benzylic alcohol, enabling direct functionalization in cross-coupling and derivatization workflows. The pendant hydroxyl group facilitates protection or oxidation to the corresponding aldehyde, while the electron-deficient heteroaryl moiety supports palladium-catalyzed transformations under standard conditions. This bench-stable reagent integrates readily into synthetic sequences requiring halogen-directed C–C or C–heteroatom bond formation.
1-(5-Bromopyridin-2-yl)ethan-1-ol serves as a versatile building block in medicinal chemistry, enabling direct incorporation of a brominated pyridine moiety into target molecules. The primary alcohol functionality facilitates efficient derivatization via esterification, etherification, or coupling reactions. Its bench-stable nature and compatibility with standard cross-coupling protocols make it well-suited for late-stage functionalization and the construction of heterocyclic scaffolds in API 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: