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Structure of 89793-11-3
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Methyl 2-chloro-6-methylpyrimidine-4-carboxylate is a bench-stable pyrimidine derivative featuring a chlorine atom at C2 and a methyl group at C6, enabling selective functionalization. The ester moiety facilitates downstream transformations in medicinal chemistry. This electron-deficient heterocycle integrates readily into complex scaffolds under standard conditions.
Methyl 2-chloro-6-methylpyrimidine-4-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. The ortho-chloro and ester functionalities facilitate palladium-catalyzed cross-coupling reactions and selective derivatization, while the methyl group enhances stability and modulates electronic properties. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for medicinal chemistry campaigns and API intermediate 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: