6-Deoxy-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose

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6-Deoxy-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose

Original price was: $995.00.Current price is: $495.00.

Catalog Number: B2027232 (1 g)
6-Deoxy-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose is a protected derivative of fucose widely utilized as a key building block in carbohydrate chemistry and complex oligosaccharide synthesis. Featuring two isopropylidene acetal protecting groups, it offers high stability and selective reactivity at the C-6 position during chemical modifications. Supplied as a high-purity research reagent, this compound is ideal for glycobiology research and the custom synthesis of bioactive novel carbohydrates. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

6-Deoxy-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose
Catalog number: B2027232
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 244.29
Supplied as: Powder
Storage: NA
Keywords: 6-Deoxy-1,2:3,4-di-O-isopropylidene-alpha-D-galactopyranose, 6-Deoxy-1,2:3,4-di-O-isopropylidene-a-D-galactopyranose, 1,2:3,4-Di-O-isopropylidene-6-deoxy-alpha-D-galactopyranose

References:
1. Roslund MU, Klika KD, Lehtilä RL, Tähtinen P, Sillanpää R, Leino R. Conformation of the Galactose Ring Adopted in Solution and in Crystalline Form as Determined by Experimental and DFT 1H NMR and Single-Crystal X-ray Analysis. Journal of Organic Chemistry. 2004;69(2):331-338.
2. Dhumure AB, Patil AB, Kulkarni AS, Voevodina I, Scandola M, Shinde VS. Thermoresponsive copolymers with pendant D-galactosyl 1,2,3-triazole groups: synthesis, characterization and thermal behavior. New Journal of Chemistry. 2015;39(10):8179-8187.
3. Aslam U, Ahmed S, Khan A, Siddiqui S. Chromatography Free Synthesis of Reversed N-Triazole Nucleosides Starting from D-Galactopyranose using 1,3-Dipolar Cycloaddition Reactions. Journal of the Chemical Society of Pakistan. 2024;46(2):187-193.
4. Lemieux RU, Alais J. The synthesis of derivatives of lactosamine and cellobiosamine to serve as probes in studies of the combining site of the monoclonal anti-I Ma antibody. Canadian Journal of Chemistry. 1984;62(2):272-280.
5. Holden HM, Rayment I, Thoden JB. Structure and function of enzymes involved in the Leloir pathway for galactose metabolism. Journal of Biological Chemistry. 2003;278(45):43885-43888.
6. Frey PA. The Leloir pathway: a century of biochemistry and genetics. FASEB Journal. 1996;10(4):461-470.
7. Timson DJ. The structural biology of galactosemia. International Journal of Molecular Sciences. 2016;17(7):1028.
8. Leloir LF. The enzymatic transformation of uridine diphosphate glucose into a galactose derivative. Archives of Biochemistry and Biophysics. 1951;33(2):186-190.
9. Coelho AI, Berry GT, Rubio-Gozalbo ME. Galactosemia: old metabolite, new implications. Journal of Inherited Metabolic Disease. 2015;38(3):431-443.
10. McCorvie TJ, Timson DJ. The structural and physiological basis of galactosemia. Biochimica et Biophysica Acta – Molecular Basis of Disease. 2011;1812(11):1385-1398.
6-Deoxy-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose

Products Related to 6-Deoxy-1,2:3,4-di-O-isopropylidene-α-D-galactopyranose can be found at Carbohydrates

Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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