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Structure of 856163-79-6
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This bench-stable, moisture-tolerant pyridylmethanol features a dual chloro substitution that enhances electrophilic reactivity. The functional group integrates readily into coupling reactions, serving as a key intermediate in the synthesis of pharmaceuticals and agrochemicals.
(4,6-Dichloropyridin-2-yl)methanol serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized intermediates. Its dichloropyridine core provides high reactivity in nucleophilic substitution reactions, particularly with amines and thiols, facilitating the rapid assembly of complex molecules. The benzylic alcohol functionality offers a handle for selective derivatization, including oxidation or protection, while maintaining compatibility with diverse reaction conditions. Bench-stable and readily purified by distillation or chromatography, it functions reliably in both small-scale synthesis and process development workflows.
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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: