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Structure of 1206968-88-8
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(5-Bromo-3-chloropyridin-2-yl)methanol features a pyridine core bearing bromo and chloro substituents at the 5- and 3-positions, respectively, with a reactive methanol group at the 2-position. This trifunctional scaffold enables direct incorporation into cross-coupling reactions and serves as a key building block in pharmaceutical synthesis. The molecule exhibits bench-stable handling under standard conditions and facilitates efficient derivatization through its hydroxymethyl moiety.
(5-Bromo-3-chloropyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient functionalization via nucleophilic substitution or coupling reactions. The pendant hydroxymethyl group facilitates derivatization to esters, ethers, or amides, while the bromo and chloro substituents support palladium-catalyzed cross-coupling processes. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical scaffold for constructing complex heterocyclic architectures.
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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: