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Structure of 944901-04-6
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This bench-stable amine features a pyrimidine core functionalized with a methoxy group at C2 and a methylamine side chain at C4. The electron-donating methoxy moiety enhances nucleophilicity, while the primary amine enables straightforward derivatization. This scaffold integrates readily into pharmaceutical intermediates and functional materials.
(2-Methoxypyrimidin-4-yl)methanamine serves as a versatile building block for medicinal chemistry and agrochemical synthesis, enabling efficient construction of pyrimidine-based scaffolds. The molecule exhibits robust bench stability and facilitates nucleophilic substitution reactions at the 4-position, while its methoxy group enhances solubility and modulates electronic properties. Its amine functionality supports straightforward derivatization via amidation, alkylation, or coupling protocols, making it ideal for high-throughput library generation and process-scale applications.
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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: