2,3,3’,4,6,6’-Hexa-O-acetyl-lactal

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2
(4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate)
2,3,3’,4,6,6’-Hexa-O-acetyl-lactal - Image 4

2,3,3’,4,6,6’-Hexa-O-acetyl-lactal

Original price was: $795.00.Current price is: $395.00.

Catalog Number: B2027243 (1 g)
2,3,3’,4,6,6’-Hexa-O-acetyl-lactal is a peracetylated derivative of lactal widely utilized as a versatile building block in carbohydrate chemistry and oligosaccharide synthesis. Featuring fully protected hydroxyl groups, it acts as a key intermediate for the stereoselective functionalization and synthesis of complex glycosides. Supplied as a high-purity reagent, this compound is suitable for advanced biochemical research. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

2,3,3’,4,6,6’-Hexa-O-acetyl-lactal
Catalog number: B2027243
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: NA
Supplied as: Powder
Storage: NA
Keywords: 2,3,3′,4,6,6′-Hexaacetyl-D-lactal, Hexa-O-acetyl-D-lactal, 2,3,3′,4,6,6′-Hexa-O-acetyl lactal, Hexa-O-acetyllactal

References:
1. Ferrier, R. J. (1969). Unsaturated carbohydrates. Part IX. Reactions of Lewis acids with acetates of D-glucal and D-galactal. Journal of the Chemical Society C: Organic, 1969, 570-574.
2. Danishefsky, S. J., & Bilodeau, M. T. (1996). Glycals in organic synthesis: The assembly of oligosaccharides belonging to the blood group family. Angewandte Chemie International Edition, 35(13-14), 1380-1419.
3. Lemieux, R. U., & Morgan, A. R. (1965). The scammonin reaction and related studies on glycals. Canadian Journal of Chemistry, 43(8), 2190-2204.
4. Toshima, K., & Tatsuta, K. (1993). Recent progress in O-glycosylation methods. Chemical Reviews, 93(4), 1503-1531.
5. Fraser-Reid, B., & Radatus, B. (1970). Synthetic applications of unsaturated sugars. Canadian Journal of Chemistry, 48(13), 2146-2152.
6. Tiwari, V. K., Mishra, B. B., Mishra, K. B., & Kapoor, R. (2012). Cu-catalyzed synthesis of glycals and their application in oligosaccharide synthesis. Carbohydrate Research, 356, 1-15.
7. Lichtenthaler, F. W. (2002). 100 years of carbohydrate chemistry: Core concepts, milestone reactions, and stereospecific synthesis. Angewandte Chemie International Edition, 41(20), 3762-3804.
8. Schmidt, R. R. (1986). New methods for the synthesis of glycosides and oligosaccharides. Angewandte Chemie International Edition, 25(3), 212-235.
9. Paulsen, H. (1982). Advances in selective chemical syntheses of complex oligosaccharides. Angewandte Chemie International Edition, 21(3), 155-173.
10. Bovin, N. V., & Khorlin, A. Y. (1985). Synthesis of oligosaccharides using O-acetylated glycals and lactals. Bioorganicheskaya Khimiya, 11(6), 780-788.
2,3,3’,4,6,6’-Hexa-O-acetyl-lactal

Products Related to 2,3,3’,4,6,6’-Hexa-O-acetyl-lactal 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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