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Structure of 2239-83-0
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2-Methyl-5-pyrimidinemethanol features a pyrimidine core functionalized with a methyl group at C2 and a hydroxymethyl substituent at C5, delivering enhanced solubility and stability. This scaffold integrates readily into heterocyclic libraries, serving as a key intermediate in medicinal chemistry campaigns targeting kinase inhibitors and nucleoside analogs.
2-Methyl-5-pyrimidinemethanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through standard functional group transformations. Its bench-stable nature and compatibility with common coupling reactions facilitate straightforward derivatization. The molecule functions effectively as a synthetic intermediate for heterocyclic compounds, particularly in the development of kinase inhibitors and nucleoside analogs.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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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-H318-H335
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Precautionary Statements : P234-P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P312-P332+P313-P362+P364-P390-P403+P233-P405-P406-P501
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Lot numbers can be found on the outside label of a product: