2,3,5-Tri-O-benzyl-b-D-ribofuranose

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2,3,5-Tri-O-benzyl-b-D-ribofuranose Basic information
Product Name:2,3,5-Tri-O-benzyl-b-D-ribofuranose
Synonyms:2,3,5-Tri-O-benzyl-b-D-ribofuranose;2,3,5-Tri-O-benzyl-beta-D-ribofuranose;β-D-Ribofuranose, 2,3,5-tris-O-(phenylmethyl)-;(2R,3R,4R,5R)-3,4-bis(benzyloxy)-5-[(benzyloxy)methyl]oxolan-2-ol;2,3,5-tri-O-benzyl-β-D-ribofuranose;2,3,5-Tri-O-benzyl-beta-D-ribofuranose-89361-52-4;(2r,3r,4r,5r)-3,4-Bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol
CAS:89361-52-4
MF:C26H28O5
MW:420.51
EINECS:
Product Categories:
Mol File:89361-52-4.mol
2,3,5-Tri-O-benzyl-b-D-ribofuranose Structure
2,3,5-Tri-O-benzyl-b-D-ribofuranose Chemical Properties
Boiling point 570.5±50.0 °C(Predicted)
density 1.21±0.1 g/cm3(Predicted)
solubility Soluble in chloroform
pka11.95±0.70(Predicted)
form Powder
color White
Safety Information
MSDS Information
2,3,5-Tri-O-benzyl-b-D-ribofuranose Usage And Synthesis
Uses2,3,5-Tris-O-(phenylmethyl)-β-D-ribofuranose 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
2,3,5-Tri-O-benzyl-b-D-ribofuranose Preparation Products And Raw materials
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