A precursor in the synthesis of nucleosides
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Product Type

Biochemicals
Synthetic Intermediates & Building Blocks

Research Area

Cancer

β-D-Ribofuranose 1,2,3,5-tetraacetate

Item No. 30408

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
1,2,3,5-tetraacetate β-D-ribofuranose
CAS Number
13035-61-5
Synonyms
  • NSC 18738
  • 1,2,3,5-tetra-O-acetyl-β-D-Ribofuranose
  • 1’,2’,3’,5’-O-tetraacetyl-β-D-Ribofuranose
Molecular Formula
C13H18O9
Formula Weight
318.3
Purity
≥98%
Formulation (Request formulation change)
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 10 mg/mlDMSO: 10 mg/mlPBS (pH 7.2): 10 mg/ml
SMILES
CC(OC[C@H]1O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H]1OC(C)=O)=O
InChi Code
InChI=1S/C13H18O9/c1-6(14)18-5-10-11(19-7(2)15)12(20-8(3)16)13(22-10)21-9(4)17/h10-13H,5H2,1-4H3/t10-,11-,12-,13-/m1/s1
InChi Key
IHNHAHWGVLXCCI-FDYHWXHSSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    5 g

    $41

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    10 g

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    25 g

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    50 g

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    Cayman Chemical
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    Product Description

    β-D-Ribofuranose 1,2,3,4-tetraacetate is a precursor in the synthesis of nucleosides with antiproliferative activity against cancer cells.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Furukawa, Y., and Honjo, M. A novel method for the synthesis of purine nucleosides using Friedel-Crafts catalysts. Chem. Pharm. Bull. (Tokyo) 16(6), 1076-1080 (1968).

    2. Wicke, L., Engels, J.W., Gambari, R., et al. Synthesis and antiproliferative activity of quinolone nucleosides against the human myelogenous leukemia k-562 cell line. Arch. Pharm. (Weinheim) 346(10), 757-765 (2013).