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Structure of 25193-95-7
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5-(Hydroxymethyl)pyrimidine features a pyrimidine core functionalized with a hydroxymethyl group, enabling direct incorporation into nucleoside analogs and bioactive heterocycles. This bench-stable derivative facilitates efficient derivatization under mild conditions, serving as a key scaffold in medicinal chemistry and agrochemical research.
5-(Hydroxymethyl)pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient functionalization at the pyrimidine C5 position. Its hydroxymethyl group facilitates oxidation to carboxylic acid, reductive amination, or etherification, supporting diverse downstream modifications. The compound exhibits good bench stability and is compatible with standard coupling and protection protocols, making it suitable for modular synthesis of heterocyclic scaffolds and API 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: