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Structure of 1046816-75-4
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2-Chloro-5-pyrimidinemethanol features a chlorinated pyrimidine core with a reactive hydroxymethyl group, enabling direct functionalization in nucleoside analog synthesis. The molecule exhibits enhanced stability under standard bench conditions and facilitates efficient coupling reactions in medicinal chemistry workflows.
2-Chloro-5-pyrimidinemethanol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the pendant hydroxymethyl functionality supports derivatization via etherification or oxidation. The compound exhibits good bench stability and is compatible with standard coupling protocols, making it well-suited for modular synthesis of heterocyclic intermediates and API candidates.
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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: