2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose

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

2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose

Original price was: $1,995.00.Current price is: $995.00.

Catalog Number: B2027229 (1 g)
2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose is a peracetylated azido-sugar derivative utilized as a versatile intermediate in carbohydrate chemistry and bioconjugation. Featuring an azido functional group at the C-2 position, it enables efficient functionalization via click chemistry for biomarker targeting. Supplied as a high-purity crystalline solid, this chemical reagent is optimized for controlled glycosylation reactions. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (2 votes)

2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose
Catalog number: B2027229
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 373.32
Supplied as: Powder
Storage: NA
Keywords: 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose, 2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-alpha-D-mannopyranose

References:
1. Pavliak V, Kovác P. A short synthesis of 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-beta-D-glucopyranose and the corresponding alpha-glucosyl chloride from D-mannose. Carbohydrate Research. 1991;210:333-337.
2. Vasella A, Witzig C, Chiara JL, Martin-Lomas M. Introduction of the azido group by azidonitration of glycals: Synthesis of 2-azido-2-deoxy-D-galactose derivatives. Helvetica Chimica Acta. 1991;74(6):1362-1375.
3. Saxon E, Bertozzi CR. Cell surface engineering by a modified Staudinger reaction. Science. 2000;287(5460):2007-2010.
4. Hang HC, Yu C, Kato DL, Bertozzi CR. A metabolic labeling approach towards proteomic analysis of mucin-type O-linked glycosylation. Proceedings of the National Academy of Sciences. 2003;100(25):14846-14851.
5. Goddard-Borger ED, Stick RV. An efficient, inexpensive, and safe azidotransfer reagent for the preparation of azides from primary amines. The Journal of Organic Chemistry. 2007;72(25):10213-10214.
6. Lemieux RU, Ratcliffe RM. The azidonitration of tri-O-acetyl-D-galactal. Canadian Journal of Chemistry. 1979;57(10):1244-1251.
7. Dube DH, Bertozzi CR. Metabolic glycan engineering as a tool to explore glycosylation. Current Opinion in Chemical Biology. 2003;7(5):616-625.
8. Laughlin ST, Bertozzi CR. Imaging the glycome in living organisms. ACS Chemical Biology. 2007;2(10):661-673.
9. Corcilius L, Santhakumar F, Payne RJ. Synthesis of azido-functionalized carbohydrates via diazotransfer. Synlett. 2013;24(18):2401-2405.
10. Zaro BW, Yang YY, Hang HC, Pratt MR. Chemical methods for detecting protein O-GlcNAcylation. FEBS Letters. 2017;591(16):2358-2370.
2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose

Products Related to 2-Azido-2-deoxy-1,3,4,6-tetra-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 - (2 votes)

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