Date published: 2025-9-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl cyanide (CAS 23316-67-8)

0.0(0)
Write a reviewAsk a question

Application:
2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl cyanide is a building block for C-nucleoside synthesis
CAS Number:
23316-67-8
Molecular Weight:
471.46
Molecular Formula:
C27H21NO7
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl cyanide is a specialized organic compound used predominantly in nucleoside synthesis, particularly for antiviral and anticancer research. Its structure, featuring a nitrile group linked to a ribofuranosyl backbone with three benzoyl protections, is crucial for the synthesis of modified nucleosides. The benzoyl groups protect the hydroxyl positions during chemical reactions, making this compound a key intermediate in the creation of nucleoside analogs that can inhibit viral replication or tumor growth at a cellular level. In biochemical research, this chemical is employed to study the interference of nucleoside analogs with DNA and RNA polymerases, which is essential for understanding the mechanisms of action of potential antiviral and anticancer agents. Its role extends to the exploration of enzyme inhibition and the metabolic pathways of nucleotide biosynthesis. The use of this compound in laboratory settings facilitates the development of novel research tools for dissecting complex biological processes, such as viral replication and cellular division, offering insights into the underlying mechanisms of disease pathology and cellular regulation.


2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl cyanide (CAS 23316-67-8) References

  1. New trends in synthesis of pyrazole nucleosides as new antimetabolites.  |  Elgemeie, GH., et al. 2005. Nucleosides Nucleotides Nucleic Acids. 24: 1227-47. PMID: 16270665
  2. A new and efficient route to the synthesis of pyrazole and pyrimidine C-nucleoside derivatives.  |  Veronese, Augusto C. and Carlo F. Morelli. 1998. Tetrahedron letters. 39.22: 3853-3856.
  3. Synthesis of 5-substituted-3-[(2′ S, 3′ S)-3′-hydroxy-2′-hydroxymethyltetrahydrofuran-3′-yl]-1, 2, 4-oxadiazoles and their epimers.  |  Wu, W. D., et al. 2000. Tetrahedron: Asymmetry. 11.7: 1527-1536.
  4. The reduction of nitriles to aldehydes: Applications of Raney nickel/sodium hypophosphite monohydrate, of Raney nickel/formic acid, or of Raney (Ni/Al) alloy/formic acid, respectively.  |  Staskun, Benjamin and Theodorus Van Es. 2008. South African Journal of Chemistry. 61: 144-156.
  5. Synthesis of β-D-ribofuranosylbenzazoles using nitrile oxide addition chemistry.  |  Smellie, Iain AS and R. Michael Paton. 2012. Arkivoc. 9: 49-61.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl cyanide, 1 g

sc-256300
1 g
$130.00