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Structure of 5018-41-7
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4-Amino-6-chloro-5-methoxypyrimidine features a strategically positioned amino group and methoxy substituent on a pyrimidine core, enabling selective coupling reactions in medicinal chemistry. The chloro handle facilitates nucleophilic substitution, while the electron-donating methoxy group enhances solubility and modulates reactivity under standard conditions. This scaffold serves as a key building block for kinase inhibitors and antiviral agents.
4-Amino-6-chloro-5-methoxypyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. Its amino and chloro groups facilitate sequential functionalization via nucleophilic substitution and coupling reactions. The methoxy group enhances solubility and modulates electronic properties, while the compound exhibits excellent bench stability and ease of purification—key advantages for high-throughput 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: