Name: 3,4-Di-O-acetyl-L-rhamnal (3,4-Di-O-acetyl-6-deoxy-L-glucal)
Brand: Molecular Depot
SKU: B2027233
Price: 595 USD
Availability: InStock
Rating: 5 (2 reviews)

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3,4-Di-O-acetyl-L-rhamnal (3,4-Di-O-acetyl-6-deoxy-L-glucal)

Original price was: $1,195.00.Current price is: $595.00.

Catalog Number: B2027233 (1 g)
3,4-Di-O-acetyl-L-rhamnal is a functionalized glycal derivative widely used as a versatile building block in organic synthesis and carbohydrate chemistry. Featuring protected hydroxyl groups, it enables selective functionalization and stereoselective glycosylation reactions for complex oligosaccharide assembly. Supplied as a high-purity chemical reagent, it is suitable for advanced research in glycobiology. Custom bulk amounts of this product are available upon request.

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In stock

SKU: B2027233 Category: Carbohydrates Tag: MD 1000

Product Description

5/5 - (2 votes)

3,4-Di-O-acetyl-L-rhamnal (3,4-Di-O-acetyl-6-deoxy-L-glucal)
Catalog number: B2027233
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 214.22
Supplied as: Powder
Storage: NA
Keywords: 3,4-Di-O-acetyl-6-deoxy-L-glucal, L-Rhamnal diacetate, Di-O-acetyl-L-rhamnal

References:
1. Holden, H. M., Rayment, I., & Thoden, J. B. Structure and function of enzymes involved in the Leloir pathway for galactose metabolism. Journal of Biological Chemistry. 2003;278(45):43885-43888.
2. Frey, P. A. The Leloir pathway: a century of biochemistry and genetics. FASEB Journal. 1996;10(4):461-470.
3. Timson, D. J. The structural biology of galactosemia. International Journal of Molecular Sciences. 2016;17(7):1028.
4. Isselbacher, K. J., Anderson, E. P., Kurahashi, K., & Kalckar, H. M. Congenital galactosemia, a single enzymatic block in galactose metabolism. Science. 1956;123(3198):635-636.
5. Coelho, A. I., Berry, G. T., & Rubio-Gozalbo, M. E. Galactosemia: old metabolite, new implications. Journal of Inherited Metabolic Disease. 2015;38(3):431-443.
6. Ning, C., & Segal, S. Plasma galactose-1-phosphate in galactoseemic patients. Journal of Inherited Metabolic Disease. 2000;23(1):32-38.
7. Leloir, L. F. The enzymatic transformation of uridine diphosphate glucose into a galactose derivative. Archives of Biochemistry and Biophysics. 1951;33(2):186-190.
8. McCorvie, T. J., & Timson, D. J. The structural and physiological basis of galactosemia. Biochimica et Biophysica Acta – Molecular Basis of Disease. 2011;1812(11):1385-1398.
9. Fridovich-Keil, J. L. Galactosemia: the good, the bad, and the unknown. Journal of Cellular Physiology. 2006;209(3):701-705.
10. Leslie, N. D. Insights into the pathogenesis of galactosemia. Annual Review of Nutrition. 2003;23(1):59-80.
3,4-Di-O-acetyl-L-rhamnal (3,4-Di-O-acetyl-6-deoxy-L-glucal)

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