Date published: 2025-12-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

3,4-Di-O-acetyl-6-deoxy-L-glucal (CAS 34819-86-8)

0.0(0)
Write a reviewAsk a question

Application:
3,4-Di-O-acetyl-6-deoxy-L-glucal is a DNA-binding agent
CAS Number:
34819-86-8
Molecular Weight:
214.22
Molecular Formula:
C10H14O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

3,4-Di-O-acetyl-6-deoxy-L-glucal is a chemical compound of interest in carbohydrate chemistry and synthetic organic chemistry research. Its chemical structure features a deoxy sugar backbone with acetyl groups at the 3 and 4 positions. This compound has been studied for its role as a key intermediate in the synthesis of various complex carbohydrates and glycoconjugates. Researchers have utilized 3,4-Di-O-acetyl-6-deoxy-L-glucal as a versatile building block for the assembly of diverse oligosaccharide structures through glycosylation reactions. Moreover, its reactivity and stereochemistry have been investigated in detail to understand its chemical behavior and selectivity in glycosylation reactions. Furthermore, this compound has been employed in the synthesis of natural products, pharmaceutical intermediates, and carbohydrate-based materials. Its ability to serve as a chiral pool starting material for the stereoselective synthesis of bioactive compounds has also been explored. Additionally, 3,4-Di-O-acetyl-6-deoxy-L-glucal has found applications in the development of new synthetic methodologies and strategies for the construction of complex carbohydrate scaffolds with potential applications in drug discovery, chemical biology, and materials science. Overall, this compound serves as a valuable tool in carbohydrate chemistry research, enabling the synthesis of diverse carbohydrate structures and contributing to advancements in various scientific fields.


3,4-Di-O-acetyl-6-deoxy-L-glucal (CAS 34819-86-8) References

  1. Stereoselective synthesis of C-[2-S-(p-tolyl)-2-thio-beta-D-galactopyranosyl] compounds using the reaction of TolSCl adducts of D-galactal with C-nucleophiles.  |  Han, M., et al. 2000. Carbohydr Res. 323: 202-7. PMID: 10782302
  2. A short and highly efficient synthesis of L-ristosamine and L-epi-daunosamine glycosides.  |  Ding, F., et al. 2011. Org Lett. 13: 652-5. PMID: 21244045
  3. Electrochemical bromochlorination of peracetylated glycals.  |  Damljanović, I., et al. 2011. Carbohydr Res. 346: 2683-7. PMID: 22015169
  4. Direct and stereoselective synthesis of 1,3-cis-3- arylsulphonaminodeoxydisaccharides and oligosaccharides.  |  Ding, F., et al. 2012. J Org Chem. 77: 5245-54. PMID: 22651548
  5. Callipeltosides A, B and C: Total Syntheses and Structural Confirmation.  |  Frost, JR., et al. 2015. Chemistry. 21: 13261-77. PMID: 26230615
  6. C-Glycopyranosyl Arenes and Hetarenes: Synthetic Methods and Bioactivity Focused on Antidiabetic Potential.  |  Bokor, É., et al. 2017. Chem Rev. 117: 1687-1764. PMID: 28121130
  7. Isolation, Structure, and Total Synthesis of the Marine Macrolide Mangrolide D.  |  Gong, J., et al. 2019. Org Lett. 21: 2957-2961. PMID: 30957503
  8. Synthesis of Benzyl 2-Deoxy-C-Glycosides.  |  Shinozuka, T. 2020. ACS Omega. 5: 33196-33205. PMID: 33403281
  9. Synthesis of the bis(cyclohexenone) core of (-)-lomaiviticin A.  |  Rose, JA., et al. 2020. Chem Sci. 11: 7462-7467. PMID: 34123029

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3,4-Di-O-acetyl-6-deoxy-L-glucal, 5 g

sc-220887
5 g
$230.00