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Structure of 4546-68-3
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This nucleoside analog features a tetrahydrofuran ring bearing a hydroxymethyl group and a purine moiety, delivering high structural fidelity for incorporation into oligonucleotide synthesis. The stereochemistry at the 2R,3S,5R positions ensures optimal conformational stability and compatibility with enzymatic processing pathways.
(2R,3S,5R)-2-(Hydroxymethyl)-5-(9H-purin-9-yl)tetrahydrofuran-3-ol serves as a key nucleoside scaffold building block, enabling efficient synthesis of purine-containing analogs via standard glycosylation protocols. Its stereochemically defined tetrahydrofuran ring and multiple hydroxyl groups facilitate selective derivatization, while its bench-stable nature supports reliable handling in multi-step synthetic sequences.
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Lot numbers can be found on the outside label of a product: