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Structure of 21950-36-7
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This purine derivative features a unique tetrahydrofuro[3,4-d][1,3]dioxole scaffold bearing a strategically positioned aminomethyl group, enabling direct integration into nucleoside analogs. The pendant amine enhances solubility and facilitates conjugation, while the rigid fused ring system ensures conformational stability under standard reaction conditions.
9-[(3aR,4R,6R,6aR)-6-(aminomethyl)-2,2-dimethyl-tetrahydro-2H-furo[3,4-d][1,3]dioxol-4-yl]-9H-purin-6-amine serves as a versatile purine scaffold for medicinal chemistry applications. Its functionalized tetrahydrofuro[3,4-d][1,3]dioxole moiety enables site-specific derivatization, while the pendant aminomethyl group facilitates conjugation or salt formation. The molecule exhibits robust bench stability and compatibility with standard peptide coupling and reductive amination protocols, making it suitable for library synthesis and target-oriented drug discovery workflows.
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Lot numbers can be found on the outside label of a product: