ChemicalBook--->CAS DataBase List--->68733-20-0

68733-20-0

68733-20-0 Structure

68733-20-0 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[HS Code ]

29400090
Hazard InformationBack 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
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