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Structure of 2168-13-0
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This pyridinol derivative features a dimethylaminomethyl group at the 2-position, enhancing solubility and nucleophilicity. The phenolic hydroxyl enables hydrogen bonding and metal chelation, while the basic pyridine nitrogen supports coordination in catalytic systems. Bench-stable and moisture-tolerant, it serves as a modular scaffold for ligands and bioactive molecule synthesis.
2-((Dimethylamino)methyl)pyridin-3-ol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds through functional group interconversions. Its pendant hydroxyl and dimethylaminomethyl groups offer orthogonal reactivity, facilitating derivatization via etherification, alkylation, or coupling reactions. The compound exhibits good bench stability and compatibility with standard purification methods, supporting its use in multi-step syntheses and API 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: