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Structure of 7461-50-9
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4-Amino-2-chloropyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, enabling direct incorporation into kinase inhibitors and antiviral agents. The amino group facilitates nucleophilic substitution, while the chloro substituent provides a reactive handle for palladium-catalyzed coupling. This molecule exhibits favorable solubility and stability under standard conditions, supporting efficient derivatization in process development workflows.
4-Amino-2-chloropyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The amino group facilitates nucleophilic substitution and coupling reactions, while the chloro substituent provides a reliable handle for palladium-catalyzed cross-coupling or displacement with diverse nucleophiles. Its bench-stable nature and compatibility with common protecting groups make it well-suited for multi-step synthesis workflows in API development.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: