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Structure of 63071-10-3
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(4-Chloropyridin-2-yl)methanol features a pyridine ring bearing a chlorine atom at the 4-position and a methanol group at the 2-position. This configuration imparts enhanced reactivity for nucleophilic substitution and facilitates incorporation into pharmaceutical intermediates. The compound exhibits bench-stable handling characteristics and demonstrates good solubility in common organic solvents, enabling seamless integration into multistep synthetic sequences.
(4-Chloropyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient functionalization via nucleophilic substitution at the chloro position. Its pyridyl methanol motif offers enhanced solubility and handles well under standard reaction conditions. The molecule functions as a key intermediate in constructing heterocyclic scaffolds and supports diverse transformations, including coupling reactions and derivatization of nitrogen-containing rings, with predictable reactivity and straightforward purification.
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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: