| Identification | Back Directory | [Name]
1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-ALPHA-D-MANNOPYRANOSE | [CAS]
68733-20-0 | [Synonyms]
-D-mannopyranose
Tetraacetylazidodeoxymannopyranose
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-&alpha
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-Mannopyranose
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-a-D-mannopyranose
2-AZIDO-2-DEOXY-1,3,4,6-TETRA-O-ACETYL-A-D-MANNOPYRANOSE
2-AZIDO-2-DEOXY-1,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSE
1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-ALPHA-D-MANNOPYRANOSE
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose ,98%
1,3,4,6-TETRA-O-ACETYL-2-AZIDO-2-DEOXY-ALPHA-D-MANNOPYRANOSE USP/EP/BP | [Molecular Formula]
C14H19N3O9 | [MDL Number]
MFCD01321201 | [MOL File]
68733-20-0.mol | [Molecular Weight]
373.32 |
| Chemical Properties | Back Directory | [Melting point ]
132 °C | [storage temp. ]
Refrigerator | [solubility ]
DMF: 30mg/mL,DMF:PBS (pH 7.2) (1:3): 0.25mg/mL,DMSO: 15mg/mL | [form ]
powder to crystal | [color ]
White to Almost white | [CAS DataBase Reference]
68733-20-0 |
| Hazard Information | Back Directory | [Description]
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is an analog of N-acetylmannosamine (ManNAc) and a building block. It has been used as a precursor in the synthesis of differently substituted trimers of the group A N. meningitidis capsular polysaccharide repeating unit for use in immunological experiments. It has also been used in the synthesis of fluorescent probes for lysosomal labeling. | [Uses]
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranose is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. | [storage]
Store at -20°C | [References]
[1] ELIANA SAXON. Investigating Cellular Metabolism of Synthetic Azidosugars with the Staudinger Ligation[J]. Journal of the American Chemical Society, 2002, 124 50: 14893-14902. DOI: 10.1021/ja027748x
[2] RIKARD SLAETTEGAARD. Synthesis of Structures Corresponding to the Capsular Polysaccharide of Neisseria meningitidis Group A.[J]. ChemInform, 2006, 37 4. DOI: 10.1002/chin.200604190
[3] NAZMIYE B YAPICI. Highly stable and sensitive fluorescent probes (LysoProbes) for lysosomal labeling and tracking.[J]. Scientific Reports, 2015: 8576. DOI: 10.1038/srep08576 |
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