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Structure of 89282-12-2
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2,4-Dihydroxy-3-nitropyridine features a pyridine core functionalized with hydroxyl groups at positions 2 and 4 and a nitro group at position 3, creating a uniquely electron-deficient heteroaromatic system. This arrangement enables participation in cross-coupling reactions and facilitates conjugation with biomolecules via its reactive nitro moiety. The compound exhibits enhanced solubility in polar solvents and stability under standard bench conditions, making it suitable for use in medicinal chemistry and materials synthesis workflows.
2,4-Dihydroxy-3-nitropyridine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to functionalized pyridine scaffolds. Its ortho-diol and nitro functionalities facilitate selective transformations, including metal-catalyzed couplings and reductive modifications. The compound exhibits bench stability and compatibility with common protecting group strategies, making it well-suited for iterative synthesis in medicinal chemistry and process development workflows.
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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: