2-Azido-2-deoxy-1,2‘,3,3‘,4‘,6,6‘-hepta-O-acetyl-α,β-lactose 2-Azido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1,3,6-tri-O-acetyl-α,β-D-glucopyranose
Original price was: $1,995.00.$995.00Current price is: $995.00.
Catalog Number: B2027228 (1 g)
2-Azido-2-deoxy-1,2′,3,3′,4′,6,6′-hepta-O-acetyl-α,β-lactose is a peracetylated azido derivative of lactose utilized as a versatile intermediate in carbohydrate chemistry and glycobiology. Featuring a reactive azido group at the C-2 position and protecting acetyl groups, it enables precise chemical functionalization and click chemistry applications to synthesize complex oligosaccharides and glycoconjugates. Supplied as a high-purity specialty reagent, this compound is primarily used in biochemical research and glycosylation studies. Custom bulk amounts of this product are available upon request.
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Product Description
2-Azido-2-deoxy-1,2‘,3,3‘,4‘,6,6‘-hepta-O-acetyl-α,β-lactose 2-Azido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1,3,6-tri-O-acetyl-α,β-D-glucopyranose
Catalog number: B2027228
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 661.58
Supplied as: Powder
Storage: NA
Keywords: 2-Azido-2-deoxy-1,2′,3,3′,4′,6,6′-hepta-O-acetyl-α,β-lactose, 2-Azido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1,3,6-tri-O-acetyl-α,β-D-glucopyranose, Hepta-O-acetyl-2-azido-2-deoxylactose
References:
1. Lemieux RU, Ratcliffe RM. The azidonitration of tri-O-acetyl-D-galactal. Canadian Journal of Chemistry. 1979;57(10):1244-1251.
2. Paulsen H. Advances in selective chemical syntheses of complex oligosaccharides. Angewandte Chemie International Edition in English. 1982;21(3):155-173.
3. Schmidt RR. New methods for the synthesis of glycosides and oligosaccharides—Are there alternatives to the Koenigs-Knorr method? Angewandte Chemie International Edition in English. 1986;25(3):212-235.
4. Toshima K, Tatsuta K. Recent progress in O-glycosylation methods. Chemical Reviews. 1993;93(4):1503-1531.
5. Danishefsky SJ, Bilodeau MT. Glycoconjugate synthesis: The glycals in the synthesis of oligosaccharides, glycopeptides, and glycolipids. Angewandte Chemie International Edition in English. 1996;35(13-14):1380-1419.
6. Sears P, Wong CH. Toward automated synthesis of oligosaccharides and glycoproteins. Science. 2001;291(5512):2344-2350.
7. Werz DB, Seeberger PH. Carbohydrate arrays as tools for glycomics. Chemistry–A European Journal. 2005;11(11):3194-3206.
8. Boltje TJ, Buskas T, Boons GJ. Opportunities and challenges in synthetic oligosaccharide assembly. Nature Chemistry. 2009;1(8):611-622.
9. Zhu X, Schmidt RR. New approaches to glycoside synthesis. Angewandte Chemie International Edition. 2009;48(11):1900-1934.
10. Panza L, Lay L. Synthesis of 2-azido-2-deoxy-glycosides and their application in oligosaccharide assembly. Journal of Carbohydrate Chemistry. 2012;31(4):275-301.
2-Azido-2-deoxy-1,2‘,3,3‘,4‘,6,6‘-hepta-O-acetyl-α,β-lactose 2-Azido-2-deoxy-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1,3,6-tri-O-acetyl-α,β-D-glucopyranose
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Additional Information
| Weight | 0.15 oz |
|---|---|
| Dimensions | 2 × 0.5 × 0.5 in |
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