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Structure of 96833-41-9
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2-Chloro-4-methoxypyrimidin-5-amine features a pyrimidine core with complementary electron-withdrawing and donor substituents, enabling selective coupling reactions in medicinal chemistry. The chloro group facilitates nucleophilic substitution, while the methoxy and amine functionalities offer orthogonal reactivity for modular derivatization. This scaffold delivers high functional group tolerance and stability under standard conditions.
2-Chloro-4-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 and methoxy functionalities provide orthogonal handles for further derivatization. The compound exhibits good bench stability and compatibility with standard coupling protocols, making it well-suited for modular synthesis of bioactive heterocycles and API intermediates.
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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: