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Structure of 36625-64-6
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2-(Hydroxymethyl)-3-nitropyridine features a pyridine ring functionalized with a hydroxymethyl group at the 2-position and a nitro group at the 3-position, delivering enhanced solubility and reactivity. This combination enables efficient incorporation into bioconjugation workflows and synthetic intermediates requiring controlled electron-withdrawing effects.
2-(Hydroxymethyl)-3-nitropyridine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to functionalized pyridine derivatives. The hydroxymethyl group facilitates selective derivatization, while the nitro functionality supports subsequent reductions and coupling reactions. Its bench-stable nature and compatibility with standard protecting group strategies make it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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: