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Structure of 91914-04-4
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3-Methylpyridin-2-ol delivers a strategically positioned hydroxyl group on a nitrogen-rich heterocycle, enabling direct incorporation into ligand architectures and catalytic scaffolds. The methyl substituent enhances electron density at the pyridinic ring while maintaining solubility in common organic solvents. This bench-stable derivative serves as a key intermediate for functionalized pyridine libraries in medicinal chemistry and materials synthesis.
3-Methylpyridin-2-ol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles through established functional group transformations. Its pyridinol scaffold offers enhanced solubility and hydrogen-bonding capacity, while the methyl group provides a site for selective oxidation or further functionalization. The compound exhibits good bench stability and compatibility with standard coupling reactions, facilitating its use in iterative synthesis 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: