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Structure of 695-85-2
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4-Chloro-5-methoxypyrimidine serves as a key heterocyclic building block in medicinal chemistry, featuring a chlorine atom at the 4-position and a methoxy group at the 5-position. This electronic configuration enables selective coupling reactions in pharmaceutical synthesis. The compound exhibits good stability under standard conditions and facilitates efficient derivatization for targeted molecular architectures.
4-Chloro-5-methoxypyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions with amines, thiols, and other heterocyclic nucleophiles, while the methoxy substituent enhances solubility and modulates electronic properties. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for modular synthesis of bioactive compounds 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: