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Allyl α-D-Galactopyranoside (CAS 48149-72-0)

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Alternate Names:
α-D-Galactose Monoallyl Ether; 2-Propen-1-yl α-D-Galactopyranoside;
Application:
Allyl α-D-Galactopyranoside is a useful synthetic intermediate for oligosaccharide synthesis
CAS Number:
48149-72-0
Molecular Weight:
220.22
Molecular Formula:
C9H16O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Allyl α-D-Galactopyranoside, a derivative of galactose, has been extensively investigated in scientific research, particularly in the fields of carbohydrate chemistry, enzymology, and food science. Its primary research applications revolve around its role as a substrate or inhibitor in enzymatic reactions involving glycoside hydrolases and glycosyltransferases. As a substrate, allyl α-D-Galactopyranoside serves as a model compound for studying the catalytic mechanisms and substrate specificity of glycoside hydrolases and glycosyltransferases. Researchers utilize techniques such as kinetic assays, X-ray crystallography, and molecular modeling to explain the molecular interactions between the compound and these enzymes, providing valuable insights into carbohydrate metabolism and biosynthesis. Moreover, allyl α-D-Galactopyranoside is employed in food science research as a flavoring agent and a precursor for the synthesis of novel food additives. Its unique chemical properties contribute to the development of natural flavors and fragrances, as well as functional food ingredients with potential health benefits. Overall, allyl α-D-Galactopyranoside serves as a valuable tool in understanding enzymatic processes and holds promise for various applications in carbohydrate-based chemistry and food science research.


Allyl α-D-Galactopyranoside (CAS 48149-72-0) References

  1. Synthesis of an artificial glycoconjugate polymer carrying Pk-antigenic trisaccharide and its potent neutralization activity against Shiga-like toxin.  |  Dohi, H., et al. 1999. Bioorg Med Chem. 7: 2053-62. PMID: 10530955
  2. Ligand recognition by the lactose permease of Escherichia coli: specificity and affinity are defined by distinct structural elements of galactopyranosides.  |  Sahin-Tóth, M., et al. 2000. Biochemistry. 39: 5097-103. PMID: 10819976
  3. A novel synthesis of alpha-D-Galp-(1-->3)-beta-D-Galp-1-O-(CH2)3-NH2, its linkage to activated matrices and absorption of anti-alphaGal xenoantibodies by affinity columns.  |  Liaigre, J., et al. 2000. Carbohydr Res. 325: 265-77. PMID: 10839120
  4. Reversed-phase high-performance liquid chromatography of peptides of porcine pepsin prepared by the use of various forms of immobilized alpha-chymotrypsin.  |  Vanková, H., et al. 2001. J Chromatogr B Biomed Sci Appl. 753: 37-43. PMID: 11302446
  5. Novel synthesis of alpha-galactosyl-ceramides and confirmation of their powerful NKT cell agonist activity.  |  Lee, A., et al. 2006. Carbohydr Res. 341: 2785-98. PMID: 17014832
  6. Double plasma treatment-induced graft polymerization of carbohydrated monomers on poly(ethylene terephthalate) fibers.  |  Bech, L., et al. 2007. Langmuir. 23: 10348-52. PMID: 17711314
  7. Stereoselective synthesis of the disaccharide unit of incednine.  |  Abbott, JR. and Roush, WR. 2013. Org Lett. 15: 62-4. PMID: 23249392
  8. Synthesis of a close analog of the repeating unit of the antifreeze glycoproteins of polar fish.  |  Anisuzzaman, AK., et al. 1988. Carbohydr Res. 174: 265-78. PMID: 3378230
  9. A simple strategy for changing the regioselectivity of glycosidase-catalysed formation of disaccharides.  |  Nilsson, KG. 1987. Carbohydr Res. 167: 95-103. PMID: 3690579

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Allyl α-D-Galactopyranoside, 1 g

sc-221238
1 g
$300.00