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Structure of 23003-35-2
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2-Bromo-6-methylpyridin-3-ol features a bromine substituent at the pyridine ring's 2-position and a methyl group at the 6-position, creating a sterically accessible site for nucleophilic substitution. The phenolic hydroxyl group enhances solubility and enables direct functionalization. This scaffold integrates readily into heterocyclic synthesis pathways, offering a stable, moisture-tolerant platform for constructing advanced intermediates in medicinal chemistry and materials science.
2-Bromo-6-methylpyridin-3-ol serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic bromine and hydroxyl functionality. The molecule exhibits good bench stability and facilitates efficient derivatization under mild conditions, making it suitable for constructing complex pyridine-based scaffolds in medicinal chemistry and agrochemical 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: