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Structure of 220770-78-5
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This boronate-bearing pyridylmethanol integrates readily into cross-coupling reactions, offering high functional group tolerance and stability under standard conditions. The electron-rich heterocyclic scaffold enhances reactivity in palladium-catalyzed transformations, while the hydroxymethyl handle enables straightforward derivatization.
(4-Bromo-3,5-dimethylpyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry and process development. The pyridine core enables transition metal-catalyzed cross-coupling reactions, while the benzylic alcohol functionality offers a direct handle for oxidation, derivatization, or incorporation into heterocyclic scaffolds. Its bench-stable nature and compatibility with standard protecting group strategies facilitate efficient synthetic sequences in API and agrochemical research.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: