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Structure of 1256789-09-9
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Methyl 6-chloro-2,4-dimethylnicotinate features a sterically hindered pyridine core with complementary electron-deficient and methyl-substituted positions. This configuration enables direct functionalization at the C-3 and C-5 sites, facilitating rapid access to diverse heterocyclic scaffolds in medicinal chemistry and agrochemical synthesis under standard conditions.
Methyl 6-chloro-2,4-dimethylnicotinate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. Its chloro and methyl substituents provide orthogonal functional handles for cross-coupling and further derivatization. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process development workflows.
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Lot numbers can be found on the outside label of a product: