3-O-Benzyl-1,2,4,6-tetra-O-acetyl-a-D-mannopyranose
3-O-Benzyl-1,2,4,6-tetra-O-acetyl-a-D-mannopyranose Basic information
- Product Name:
- 3-O-Benzyl-1,2,4,6-tetra-O-acetyl-a-D-mannopyranose
- Synonyms:
-
- 1,2,4,6-Tetra-O-acetyl-3-O-benzyl-a-D-mannopyranose
- 3-O-(PhenylMethyl)-α-D-Mannopyranose Tetraacetate
- 1,2,4,6-Tetra-O-acetyl-3-O-benzyl-α-D-mannopyranose
- α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate
- 3-O-Benzyl-1,2,4,6-tetra-O-acetyl-α-D-mannopyranose
- (2R,3S,4S,5R,6R)-6-(acetoxymethyl)-4-(benzyloxy)tetrahydro-2H-pyran-2,3,5-triyl triacetate
- 3-O-Benzyl-1,2,4,6-tetra-O-acetyl-α-D-mannopyranose, CAS 65827-58-9
- 1,2,4,6-Tetra-O-acetyl-3-O-benzyl-alpha-D-mannopyranose
- CAS:
- 65827-58-9
- MF:
- C21H26O10
- MW:
- 438.43
- Product Categories:
-
- Carbohydrates & Derivatives
- 13C & 2H Sugars
- Mol File:
- 65827-58-9.mol
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3-O-Benzyl-1,2,4,6-tetra-O-acetyl-a-D-mannopyranose Chemical Properties
- solubility
- soluble in Acetone, Chloroform, Dichloromethane,Ethanol, Ethyl Acetate, Methanol
- form
- oil
- color
- Clear Colourless
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3-O-Benzyl-1,2,4,6-tetra-O-acetyl-a-D-mannopyranose Usage And Synthesis
Chemical Properties
Oil
Uses
α-D-Mannopyranose, 3-O-(phenylmethyl)-, 1,2,4,6-tetraacetate 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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