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Structure of 15846-19-2
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4-Chloro-6-methoxypyrimidin-5-amine features a pyrimidine core functionalized with chlorine and methoxy groups, enabling selective coupling in heterocyclic synthesis. The amine moiety provides a reactive handle for derivatization, while the electron-withdrawing chlorine enhances regioselectivity in cross-coupling reactions. This compound serves as a key intermediate in medicinal chemistry and agrochemical development.
4-Chloro-6-methoxypyrimidin-5-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions, while the amine functionality supports coupling and derivatization under standard conditions. The methoxy substituent enhances solubility and modulates electronic properties, contributing to favorable reactivity profiles. This compound exhibits bench stability and is readily purified by recrystallization or column chromatography, making it well-suited for high-throughput synthesis and process development workflows.
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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: