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Structure of 2382-10-7
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2,6-Dichloro-9-methyl-9H-purine is a sterically hindered purine derivative featuring two chlorine substituents at the 2- and 6-positions and a methyl group at the 9-position. This configuration imparts enhanced stability and electron-deficient character, enabling its use as a key scaffold in nucleoside analog synthesis and medicinal chemistry applications.
2,6-Dichloro-9-methyl-9H-purine serves as a versatile building block in purine-based synthesis, enabling efficient access to substituted nucleoside analogs and heterocyclic scaffolds. Its dichloro substitution pattern facilitates regioselective functionalization at C2 and C6, while the methyl group at C9 enhances stability and modulates reactivity. The compound exhibits excellent bench stability, tolerates diverse reaction conditions, and simplifies purification—making it ideal for medicinal chemistry campaigns and API intermediate development.
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Lot numbers can be found on the outside label of a product: