Date published: 2026-5-15

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1,6-Anhydro-3,4-O-isopropylidene-β-D-galactopyranose (CAS 52579-97-2)

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CAS Number:
52579-97-2
Molecular Weight:
202.20
Molecular Formula:
C9H14O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1,6-Anhydro-3,4-O-isopropylidene-β-D-galactopyranose has emerged as a crucial compound in carbohydrate chemistry and glycobiology research. Its chemical structure, featuring an anhydrogalactose moiety with an isopropylidene protecting group, imparts unique reactivity and functionality that researchers have leveraged for various applications. One notable mechanism of action involves its utility as a key building block in the synthesis of complex carbohydrates and glycoconjugates. Chemists employ this compound as a versatile precursor to introduce galactose units into oligosaccharide and polysaccharide structures, facilitating the preparation of structurally diverse carbohydrates with precise control over regio- and stereochemistry. Additionally, 1,6-Anhydro-3,4-O-isopropylidene-β-D-galactopyranose serves as a valuable tool in carbohydrate-based drug discovery and vaccine development. Researchers utilize its synthetic accessibility and unique structural features to design and develop carbohydrate-based glycomimetics, and glycoconjugate vaccines targeting various pathogens, cancer cells, and immune-related disorders. Furthermore, its derivatives and analogs have been investigated to enhance binding affinity, pharmacokinetic properties, and immunogenicity, paving the way for the development of novel carbohydrate-based vaccines. Overall, 1,6-Anhydro-3,4-O-isopropylidene-β-D-galactopyranose plays a pivotal role in advancing research in carbohydrate chemistry, glycobiology, and biomedical sciences, offering promising opportunities for diagnostic applications.


1,6-Anhydro-3,4-O-isopropylidene-β-D-galactopyranose (CAS 52579-97-2) References

  1. Studies on the synthesis of 1,2-cis pentofuranosides from S-glycofuranosyl dithiocarbamates, dithiocarbonates and phosphorodithioates.  |  Bogusiak, J. and Szeja, W. 2001. Carbohydr Res. 330: 141-4. PMID: 11217957
  2. Three 1,6-anhydro-beta-D-glycopyranose derivatives.  |  Foces-Foces, C. 2001. Acta Crystallogr C. 57: 298-301. PMID: 11250585
  3. Glycosyl iodides are highly efficient donors under neutral conditions.  |  Hadd, Michael J. and Jacquelyn Gervay. 1999. Carbohydrate research. 320.1-2: 61-69.
  4. Synthesis of unstable 4-benzoyl-1, 6-anhydro-3-keto-β-D-mannopyranose via stereoselective photobromination of 2, 3-isopropylidene-4-benzoyl-1, 6-anhydro-β-D-mannopyranose.  |  Mahdi, Jassem G., et al. 2020. Journal of Carbohydrate Chemistry. 39.1: 24-35.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1,6-Anhydro-3,4-O-isopropylidene-β-D-galactopyranose, 500 mg

sc-220568
500 mg
$480.00