| Identification | Back Directory | [Name]
1-O-Acetyl-2,3,5-tri-O-benzyl-D-ribofuranose | [CAS]
58381-23-0 | [Synonyms]
1-O-ACETYL-2,3,5-TRI-O-BENZYL-D-RIBOFURANOSE
2,3,5-Tris-O-(phenylMethyl)-D-ribofuranose Acetate
1-O-Acetyl-2,3,5-tri-O-benzyl-D-ribofuranose min. 98%
(3R,4R,5R)-3,4-bis(benzyloxy)-5-(benzyloxymethyl)tetrahydrofuran-2-yl acetate | [Molecular Formula]
C28H30O6 | [MDL Number]
MFCD00135028 | [MOL File]
58381-23-0.mol | [Molecular Weight]
462.53 |
| Chemical Properties | Back Directory | [Appearance]
Yellow Oil | [Boiling point ]
575.655±50.00 °C(Press: 760.00 Torr)(predicted) | [density ]
1.207±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | [storage temp. ]
Refrigerator | [solubility ]
Chloroform, Ethyl Acetate | [form ]
Oil | [color ]
Yellow | [InChIKey]
CPWPSDGLXXKBKZ-STQJPMTFSA-N | [SMILES]
C1(OC(=O)C)O[C@H](COCC2=CC=CC=C2)[C@@H](OCC2=CC=CC=C2)[C@H]1OCC1=CC=CC=C1 | [CAS DataBase Reference]
58381-23-0 |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow Oil | [Uses]
D-Ribofuranose,2,3,5-tris-O-(phenylmethyl)-,1-acetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1]. | [References]
[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922 |
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| Company Name: |
J & K SCIENTIFIC LTD.
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| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
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