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Atomfair N-[9-[5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide C17H17N5O3

Description N-[9-[5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide (CAS No. 77244-86-1) is a high-purity synthetic nucleoside analogue with the molecular formula C17H17N5O3. This compound features a benzamide group attached to a purine base, which is further linked to a hydroxymethyl-substituted oxolane (tetrahydrofuran) ring. Its unique structure makes it valuable for research in medicinal chemistry, nucleoside biochemistry, and drug discovery. Available in quantities from milligrams to grams, this product is rigorously characterized by HPLC, NMR, and mass spectrometry to ensure ??95% purity. Ideal for studying enzyme interactions, antiviral mechanisms, or as a building block for novel therapeutics. Store at -20??C under inert conditions for optimal stability.

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Description

Description

N-[9-[5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide (CAS No. 77244-86-1) is a high-purity synthetic nucleoside analogue with the molecular formula C17H17N5O3. This compound features a benzamide group attached to a purine base, which is further linked to a hydroxymethyl-substituted oxolane (tetrahydrofuran) ring. Its unique structure makes it valuable for research in medicinal chemistry, nucleoside biochemistry, and drug discovery. Available in quantities from milligrams to grams, this product is rigorously characterized by HPLC, NMR, and mass spectrometry to ensure ??95% purity. Ideal for studying enzyme interactions, antiviral mechanisms, or as a building block for novel therapeutics. Store at -20??C under inert conditions for optimal stability.

  • CAS No: 77244-86-1
  • Molecular Formula: C17H17N5O3
  • Molecular Weight: 339.3
  • Exact Mass: 339.13313942
  • Monoisotopic Mass: 339.13313942
  • IUPAC Name: N-[9-[5-(hydroxymethyl)oxolan-2-yl]purin-6-yl]benzamide
  • SMILES: C1CC(OC1CO)N2C=NC3=C(N=CN=C32)NC(=O)C4=CC=CC=C4
  • Synonyms: NSC613006, SCHEMBL19343832, NSC-613006

Application

This compound serves as a key intermediate in the synthesis of modified nucleosides with potential antiviral or anticancer activity. Researchers utilize it to investigate purine metabolism enzymes, such as nucleoside phosphorylases. Its structural features make it valuable for probing DNA/RNA-protein interactions in biochemical assays. The hydroxymethyl group provides a handle for further chemical modifications in drug development projects.

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