Date published: 2026-6-8

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Methyl Fucopyranoside (CAS 65310-00-1)

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Alternate Names:
Methyl 6-Deoxy-galactopyranoside
Application:
Methyl Fucopyranoside is an α,β mixture of a modified fucopyranoside
CAS Number:
65310-00-1
Molecular Weight:
178.18
Molecular Formula:
C7H14O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methyl Fucopyranoside is a synthetic derivative of the naturally occurring deoxy sugar fucose, which is linked to a methyl group through a glycosidic bond. This compound serves as an essential tool in glycoscience for the study of glycosidic linkage properties and the behavior of fucose in biological systems. The methyl group at the anomeric carbon stabilizes the glycosidic bond, making methyl fucopyranoside a valuable model compound in enzymatic studies and in the synthesis of larger, more complex oligosaccharides. In research, methyl fucopyranoside is utilized extensively to explore the stereochemical aspects of fucosylation reactions. Fucosylation is a critical type of glycosylation that impacts cell-cell interaction, signal transduction, and immune response in living organisms. By studying how methyl fucopyranoside interacts with fucosyltransferases, researchers can gain insights into the enzymatic mechanisms that control the biosynthesis of fucosylated glycoconjugates. Additionally, this compound is also employed in studies focusing on the physical and chemical properties of fucose-containing structures, particularly their stability, reactivity, and interaction with other biological molecules. Understanding these interactions helps in elucidating the role of fucose in biological systems and contributes to the development of biomimetic materials and synthetic pathways that could harness the unique properties of fucose in industrial and biotechnological applications.


Methyl Fucopyranoside (CAS 65310-00-1) References

  1. Recognition of selected monosaccharides by Pseudomonas aeruginosa Lectin II analyzed by molecular dynamics and free energy calculations.  |  Mishra, NK., et al. 2010. Carbohydr Res. 345: 1432-41. PMID: 20546713
  2. Mass spectra of some labda-7,14-dien-13(R)-ol monoglycosides under electron impact  |  Eguchi, S., Uchio, Y., & Nakayama, M. 1983. Biomedical Mass Spectrometry. 10(6): 363-368.
  3. Structure of desacylsaponins obtained from the bark of Quillaja saponaria  |  Higuchi, R., Tokimitsu, Y., Fujioka, T., Komori, T., Kawasaki, T., & Oakenful, D. G. 1986. Phytochemistry. 26(1): 229-235.
  4. Complexation-induced activation of sugar OH groups. Regioselective alkylation of methyl fucopyranoside via cyclic phenylboronate in the presence of amine  |  Oshima, K., Kitazono, E. I., & Aoyama, Y. 1997. Tetrahedron letters. 38(28): 5001-5004.
  5. Synthesis of Hexane-Tetrols and -Triols with Fixed Hydroxyl Group Positions and Stereochemistry from Methyl Glycosides over Supported Metal Catalysts  |  Krishna, S. H., Cao, J., Tamura, M., Nakagawa, Y., De Bruyn, M., Jacobson, G. S.,.. & Huber, G. W. 2019. ACS sustainable chemistry & engineering. 8(2): 800-805.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl Fucopyranoside, 1 g

sc-221928
1 g
$190.00