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Structure of 26452-81-3
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4-Chloro-6-methoxypyrimidine features a pyrimidine core with complementary electron-withdrawing and donating substituents, enabling selective functionalization at C5. This bench-stable heterocycle integrates efficiently into pharmaceutical intermediates, where the chlorine facilitates nucleophilic substitution and the methoxy group enhances solubility and regiocontrol during synthesis.
4-Chloro-6-methoxypyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The chloro group at C4 facilitates nucleophilic substitution reactions with amines, thiols, and other heteroatom nucleophiles, while the methoxy substituent at C6 enhances solubility and modulates electronic properties. This compound exhibits excellent bench stability and compatibility with standard coupling protocols, making it well-suited for modular synthesis of bioactive molecules 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: