1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose

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(4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate)

1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose

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

Catalog Number: B2027265 (1 g)
1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose is a fully acetylated carbohydrate derivative that functions as a key protected sugar building block in carbohydrate chemistry and organic synthesis. Supplied as a high-purity crystalline solid, it is commonly utilized for stereoseospecific glycosylation reactions and the synthesis of complex oligosaccharides or glycoconjugates. It plays a critical role in biochemical research, particularly in the study of glycosylation pathways and selectin-mediated cell adhesion. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose
Catalog number: B2027265
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 390.35
Supplied as: Powder
Storage: NA
Keywords: α-D-Mannose pentaacetate, 1,2,3,4,6-PENTA-O-ACETYL-ALPHA-D-MANNOPYRANOSE, ALPHA-D-MANNOSE PENTAACETATE, A-D-mannosepentaacetate

References:
1. Lemieux RU, Shyluk WP. The preparation of alpha-D-mannopyranose pentaacetate. Canadian Journal of Chemistry. 1953;31(6):528-535.
2. Wolfrom ML, Thompson A. Acetylation of D-mannose. Methods in Carbohydrate Chemistry. 1963;2:211-215.
3. Schmidt RR, Michel J. Facile synthesis of alpha- and beta-O-glycosides of D-mannose. Angewandte Chemie International Edition in English. 1980;19(9):731-732.
4. Crich D, Sun S. Direct synthesis of beta-mannopyranosides. Journal of the American Chemical Society. 1997;119(46):11217-11223.
5. Toshima K, Tatsuta K. Recent progress in O-glycosylation methods. Chemical Reviews. 1993;93(4):1503-1531.
6. Paulsen H. Advances in selective chemical syntheses of complex oligosaccharides. Angewandte Chemie International Edition in English. 1982;21(3):155-173.
7. Garegg PJ. Thioglycosides as glycosyl donors in oligosaccharide synthesis. Advances in Carbohydrate Chemistry and Biochemistry. 1997;52:179-205.
8. Davis BG. Recent developments in chemical glycosylation. Journal of the Chemical Society, Perkin Transactions 1. 2000;(14):2137-2160.
9. Barresi F, Hindsgaul O. Improved synthesis of beta-D-mannopyranosides. Journal of the American Chemical Society. 1991;113(24):9376-9377.
10. Kartha KPR, Field RA. Iodine and its interhalogen compounds: versatile reagents for carbohydrate synthesis. Carbohydrate Letters. 1998;3(1):33-40.
1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose

Products Related to 1,2,3,4,6-Penta-O-acetyl-α-D-mannopyranose 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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