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Structure of 127861-30-7
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Methyl 2-chloro-6-methoxypyrimidine-4-carboxylate is a bench-stable pyrimidine derivative featuring a chloro group at C2 and a methoxy substituent at C6, enabling selective functionalization in heterocyclic synthesis. The ester handle facilitates downstream transformations, while the electron-deficient ring system supports nucleophilic substitution reactions under mild conditions.
Methyl 2-chloro-6-methoxypyrimidine-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its reactive chloro group facilitates nucleophilic substitution under mild conditions, while the ester functionality supports further derivatization. The molecule exhibits good bench stability and is compatible with common functional groups, making it well-suited for medicinal chemistry campaigns and process-scale applications.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: