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1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose, 98%|923179|13035-61-5

1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose, 98%

Cat. No JK923179_500_G
J&K Chemical

Product Information

Product Name
1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose, 98%
Brand Name
J&K
Product Number
923179
CAS
13035-61-5
Molecular Formula
C13H18O9
Molecular Weight
318.28
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
  • Tetra-O-acetyl-β-D-ribofuranose
  • β-D-Ribofuranose 1,2,3,5-Tetraacetate
PubChem CID
83064
IUPAC Name
(2R,3R,4R,5S)-3,4,5-triacetyloxyoxolan-2-ylmethyl acetate
InChI Key
IHNHAHWGVLXCCI-FDYHWXHSSA-N
SMILES
CC(=O)OCC@@H1C@H(C@H(C@@H(O1)OC(=O)C)OC(=O)C)OC(=O)C

Properties

Melting Point
81-83

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
H336
Precautionary Statement
P280
P305+P351+P338
P264+P265
P337+P317
Storage Condition
Store at 2-8℃

References Data Source From Pubchem

Biomimetic direct hydroperoxidation of unactivated C(sp3)–H bonds enables effective functionalization of diverse types of natural products and/or drugs
Publication Name: Science China Chemistry
Publication Date: 2025-12-10
DOI: 10.1007/s11426-025-3028-6

Methods for Industrial Scale Preparation and Purification of Nicotinamide Coenzymes and Their Precursors
Publication Name: Biology of Nicotinamide Coenzymes
Publication Date: 2025
DOI: 10.1007/978-981-97-9877-3_45

Synthesis and antiviral activity of homodimers of 1,2,3-triazolyl nucleoside analogs
Publication Name: Russian Chemical Bulletin
Publication Date: 2024-06
DOI: 10.1007/s11172-024-4296-5

Cytotoxicity Studies of 5-Arylaminouracil Derivatives
Publication Name: Molecular Biology
Publication Date: 2024-04
DOI: 10.1134/s0026893324020079

Synthesis and Antiviral Activity of New Dimeric 1,2,3-Triazolyl Pyrimidine Nucleoside Analogues
Publication Name: Russian Journal of Organic Chemistry
Publication Date: 2024-04
DOI: 10.1134/s1070428024040031

1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose, 98%

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