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Structure of 22536-65-8
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2-Chloro-5-methoxypyrimidine features a reactive chlorine atom at the 2-position paired with a methoxy group at the 5-position, enabling selective functionalization in heterocyclic synthesis. This electron-deficient pyrimidine scaffold supports efficient coupling reactions under mild conditions, delivering key intermediates for pharmaceuticals and agrochemicals.
2-Chloro-5-methoxypyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its chloro group facilitates nucleophilic substitution reactions with amines, thiols, and other heteroatoms, while the methoxy substituent enhances solubility and modulates electronic properties. This compound exhibits good bench stability and is compatible with standard coupling protocols, making it well-suited for parallel synthesis campaigns and scale-up applications.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: