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Structure of 51834-97-0
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5-Hydroxy-2-methoxylpyridine features a pyridine core functionalized with hydroxyl and methoxy groups at the 5- and 2-positions, respectively. This arrangement imparts enhanced solubility and polarity, facilitating use in cross-coupling reactions and as a building block in medicinal chemistry. The molecule exhibits stability under standard bench conditions and serves as a scaffold for bioactive compound synthesis.
5-Hydroxy-2-methoxypyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to bioactive scaffolds through established functional group transformations. Its ortho-difunctionalized pyridine core supports selective derivatization, including Suzuki-Miyaura coupling and electrophilic substitution, while the hydroxyl and methoxy groups offer complementary reactivity for orthogonal protection strategies. Bench-stable and amenable to purification via standard chromatographic methods, it functions reliably in multi-step syntheses of pharmaceutical intermediates.
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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: