CAS 13035-61-5
:β-D-Ribofuranose, 1,2,3,5-tetraacetate
Description:
β-D-Ribofuranose, 1,2,3,5-tetraacetate is a derivative of ribofuranose, a sugar component of RNA. This compound features a furanose ring structure, which is a five-membered ring containing four carbon atoms and one oxygen atom. The tetraacetate designation indicates that four hydroxyl groups on the ribofuranose have been acetylated, enhancing its lipophilicity and stability. This modification can influence its reactivity and solubility in organic solvents. The compound is typically used in biochemical research and synthesis, particularly in studies involving nucleic acids and carbohydrate chemistry. Its CAS number, 13035-61-5, uniquely identifies this specific chemical substance in databases. The acetylation process can also affect the compound's biological activity, making it a useful tool in various applications, including drug design and development. Overall, β-D-Ribofuranose, 1,2,3,5-tetraacetate serves as an important intermediate in the synthesis of more complex biomolecules.
Formula:C13H18O9
InChI: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:InChIKey=IHNHAHWGVLXCCI-FDYHWXHSSA-N
SMILES:O(C(C)=O)[C@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)O[C@@H]1COC(C)=O
Synonyms:- 1,2,3,5-Tetra-O-Acetyl-D-Ribose
- 1,2,3,5-Tetra-O-acetyl-D-ribofuranose
- 1,2,3,5-Tetra-O-acetyl-β-<span class="text-smallcaps">D</span>-ribofuranose
- 1,2,3,5-Tetra-O-acetyl-β-<span class="text-smallcaps">D</span>-ribose
- 1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose
- 1,2,3,5-Tetraacetyl-β-<span class="text-smallcaps">D</span>-ribofuranose
- 1,2,3,5-tetra-O-acetyl-beta-D-ribofuranose
- 1,2,3,5-tetra-O-acetylpentofuranose
- 1,2,3,5-tetraacetyl-beta-D-ribofuranose
- 1,2,3,5-tetraacetyl-beta-D-ribose
- 1β-<span class="text-smallcaps">D</span>-Tetraacetylribose
- NSC 18738
- Ribofuranose, tetraacetate, β-<span class="text-smallcaps">D</span>-
- Tetra-O-acetyl-β-<span class="text-smallcaps">D</span>-ribofuranose
- Tetraacetyl-β-<span class="text-smallcaps">D</span>-ribofuranose
- Tetraacetylribofuranose
- Tetraacetylribose
- [(2S,5R)-3,4-diacetoxy-5-(acetoxymethyl)tetrahydrofuran-2-yl] acetate
- β-<span class="text-smallcaps">D</span>-Ribofuranose, 1,2,3,5-tetraacetate
- β-<span class="text-smallcaps">D</span>-Ribofuranose, tetraacetate
- β-D-Ribofuranose 1,2,3,5-tetraacetate
- β-Ribofuranose-1,2,3,5-tetraacetate
- Tetra-O-acetyl-β-D-ribofuranose
- β-D-Ribofuranose, tetraacetate
- beta-D-Ribofuranose 1,2,3,5-tetraacetate
- See more synonyms
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Found 15 products.
Tetra-O-acetyl-β-D-ribofuranose
CAS:Formula:C13H18O9Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:318.28β-D-Ribofuranose 1,2,3,5-tetraacetate, 98+%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C13H18O9Purity:98+%Color and Shape:Crystals or powder or crystalline powder, WhiteMolecular weight:318.28β-D-Ribofuranose 1,2,3,5-Tetraacetate
CAS:Formula:C13H18O9Purity:98%Color and Shape:SolidMolecular weight:318.2766Ref: IN-DA003O64
1kg47.00€25gTo inquire5kg117.00€100g25.00€250g26.00€25kg543.00€500g33.00€50kgTo inquireRibavirin Impurity 2
CAS:Formula:C13H18O9Color and Shape:White To Off-White SolidMolecular weight:318.281,2,3,5-Tetra-O-acetyl-b-D-ribofuranose
CAS:Formula:C13H18O9Purity:≥ 98.0%Color and Shape:White to off-white powderMolecular weight:318.28β-D-Ribofuranose 1,2,3,5-tetraacetate
CAS:<p>β-D-Ribofuranose 1,2,3,4-tetraacetate is a precursor in the synthesis of nucleosides with antiproliferative activity against cancer cells.1,2</p>Formula:C13H18O9Color and Shape:White To Yellowish CrystalMolecular weight:318.281,2,3,5-Tetra-O-acetyl-β-D-ribofuranose
CAS:<p>1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose</p>Purity:98%Color and Shape:Off-White SolidMolecular weight:318.28g/mol1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose
CAS:<p>Important resource for RNA- and DNA-related syntheses including ribosylation</p>Formula:C13H18O9Purity:Min. 95%Color and Shape:White PowderMolecular weight:318.28 g/mol1,2,3,5-Tetraacetyl-ß-D-ribofuranose
CAS:Formula:C13H18O9Purity:98%Color and Shape:SolidMolecular weight:318.2781,2,3,5-Tetra-O-acetyl b-D-Ribofuranose
CAS:Controlled Product<p>Applications Used in the synthesis of 3-(β-D-ribofuranosyl)-2,3-dihydro-6H-1,3-oxazine-2,6-dione, a new pyrimidine nucleoside analog related to uridine.<br>References Chwang, T.-L., et al.: J. Med. Chem., 19, 643 (1976),<br></p>Formula:C13H18O9Color and Shape:NeatMolecular weight:318.281,2,3,5-Tetra-O-Acetyl-b-D-Ribofuranose extrapure, 98%
CAS:Formula:C13H18OPurity:min. 98%Color and Shape:White to Off white, Crystalline powder, Clear, Colourless to Pale yellowMolecular weight:318.281,2,3,5-Tetra-O-acetyl β-D-Ribofuranose-13C5
CAS:Controlled Product<p>Applications 1,2,3,5-Tetra-O-acetyl β-D-Ribofuranose-13C5 is an intermediate used in the synthesis of Ribavirin-13C5 (R414477), which is a labeled Rivavirin. Purine nucleoside analog; inhibits inosine monophosphate dehydrogenase (IMPDH). Used as an antiviral agent.This compound is suitable for pyruvate dehydrogenase (PDH) related research.<br>References Fernandez, H., et al.: Eur. J. Epidemiol., 2, 1 (1986), Liao, H.J. and Stollar, V.: Antiviral Res., 22, 285 (1993), Honda, Y., et al.: Antimicrob. Agents Chemother., 38, 653 (1994), Reichard, O., et al.: Lancet, 351, 83 (1998)<br></p>Formula:C5C8H18O9Color and Shape:NeatMolecular weight:323.241,2,3,5-Tetra-O-acetyl-β-D-ribofuranose
CAS:<p>1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose is a sugar that has been acetylated at the hydroxyl group. It has biological properties that are similar to those of 1,2,3,5-tetraacetyl-β-D-ribofuranose. This compound is an analog of 1,2,3,5-tetraacetyl-β-D-ribofuranose and can be used as a model system for studying the effects of acetylation on the properties of this molecule. Acetylation at the hydroxyl group in sugars can lead to low energy (chemical) properties. The acetylated form of this compound reacts with trifluoromethanesulfonic acid to give tetrafluoroethylene and ammonium sulfate in a model reaction solution. 1,2,3,5-Tetraacetyl β</p>Formula:C13H18O9Purity:Min. 97.5 Area-%Molecular weight:318.28 g/molRef: 3D-T-1760
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