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Structure of 51035-70-2
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5-(Hydroxymethyl)pyridin-3-ol features a pyridine ring bearing both hydroxyl and hydroxymethyl groups at meta positions, enabling dual functionalization. This bifunctional scaffold integrates readily into synthetic sequences requiring polar, electron-rich sites. The compound demonstrates stability under standard conditions and supports efficient derivatization in medicinal chemistry and materials synthesis.
5-(Hydroxymethyl)pyridin-3-ol serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its pyridine core provides a platform for metal-catalyzed coupling reactions, while the ortho-hydroxyl and hydroxymethyl groups enable efficient derivatization via etherification, oxidation, or protection strategies. The molecule exhibits good bench stability and facilitates straightforward purification, making it suitable for iterative synthetic sequences in medicinal chemistry 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: