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Structure of 4763-36-4
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4-Chloro-5-methoxypyrimidin-2-amine features a pyrimidine core functionalized with chlorine and methoxy groups, enabling selective coupling in heterocyclic synthesis. The amine handle facilitates conjugation, while the electron-deficient ring enhances reactivity in transition-metal-catalyzed transformations. This bench-stable intermediate supports efficient access to bioactive compounds in medicinal chemistry.
4-Chloro-5-methoxypyrimidin-2-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 methoxy and amino functionalities offer orthogonal reactivity for downstream derivatization. The compound exhibits excellent bench stability and is compatible with standard coupling protocols, making it well-suited for parallel synthesis and API 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: