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Structure of 15846-15-8
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4,6-Dimethoxypyrimidin-5-amine features a pyrimidine core bearing two methoxy groups and a primary amine at the 5-position, enabling efficient coupling in heterocyclic synthesis. The electron-donating methoxy substituents enhance nucleophilicity at the amine site, while the scaffold exhibits stability under standard reaction conditions. This compound serves as a key intermediate in medicinal chemistry and agrochemical development.
4,6-Dimethoxypyrimidin-5-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its ortho-dimethoxy substitution pattern enhances stability and facilitates nucleophilic displacement reactions. The amine functionality provides a direct handle for coupling reactions, including amidation and urea formation, supporting rapid diversification in target molecule synthesis. Well-suited for bench-scale applications, it exhibits good solubility and purification compatibility.
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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: