1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose

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1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose

Original price was: $795.00.Current price is: $395.00.

Catalog Number: B2027275 (1 g)
1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose is a peracetylated ribose derivative widely used as a key intermediate in organic chemistry and biochemistry. Featuring protective acetyl groups on its hydroxyl functionalities, it offers enhanced stability and solubility for synthetic applications such as nucleoside, nucleotide, and carbohydrate synthesis. Supplied as a high-purity crystalline solid, this versatile reagent is essential for chemical biology. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose
Catalog number: B2027275
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 318.28
Supplied as: Powder
Storage: NA
Keywords: β-D-Ribofuranose 1,2,3,5-Tetraacetate, 1,2,3,5-Tetraacetyl-beta-D-ribofuranose, 1,2,3,5-Tetra-O-acetyl-β-D-ribose, Tetraacetyl-β-D-ribofuranose, 1β-D-Tetraacetylribose, NSC 18738

References:
1. Guthrie RD, Smith SC. Carbohydrate derivatives of biological interest. Part I. Synthesis of 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose and related derivatives. Journal of the Chemical Society. 1968:1342-1347.
2. Vorbrüggen H, Krolikiewicz K, Bennua B. Nucleoside synthesis with trimethylsilyl triflate and other silyl perfluoroalkanesulfonates in glycosylation reactions. Chemische Berichte. 1981;114(4):1237-1255.
3. Reist EJ, Benitez A, Goodman L, Baker BR. Potential anticancer agents. LX. Synthesis of 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose and derived nucleosides. Journal of Organic Chemistry. 1962;27(9):3274-3279.
4. Zinner H, Nimz H. Synthese von 1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose aus D-Ribose. Chemische Berichte. 1959;92(8):1930-1933.
5. Vorbrüggen H, Ruh-Pohlenz C. Handbook of Nucleoside Synthesis. John Wiley & Sons. 2001;12:45-89.
6. Montgomery JA, Thomas HJ. Synthesis of potential anticancer agents. XX. Preparation of nucleosides of 6-chloropurine using 1,2,3,5-tetra-O-acetyl-D-ribofuranose. Journal of the American Chemical Society. 1959;81(14):3714-3717.
7. Niedballa U, Vorbrüggen H. A general synthesis of N-glycosides. I. Synthesis of pyrimidine nucleosides using 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose. Journal of Organic Chemistry. 1974;39(25):3654-3660.
8. Stevens CL, Blumbergs P, Wood DL. Stereospecific synthesis of β-D-ribofuranosyl nucleosides via tetra-O-acetyl-D-ribofuranose. Journal of Organic Chemistry. 1966;31(10):3122-3128.
9. Noyori R, Kurimoto I. Catalytic condensation of 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose with silylated nucleobases. Tetrahedron Letters. 1986;27(11):1281-1284.
10. Winkley MW, Robins RK. Direct glycosylation of purines with 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose in the synthesis of ribonucleosides. Journal of Organic Chemistry. 1968;33(7):2822-2827.
1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose

Products Related to 1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose can be found at Carbohydrates

Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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