| Identification | Back Directory | [Name]
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-D-galactopyranose | [CAS]
84278-00-2 | [Synonyms]
2-Azido-D-galactose tetraacetate
2-Azido-2-deoxy-D-galactose tetraacetate
2-Azido-D-galactose tetraacetate >=97% (HPLC)
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-D-galactose
2-Azido-2-deoxy-D-galactopyranose 1,3,4,6-Tetraacetate
2-Azido-2-deoxy-3,4,6-tri-O-acetyl-D-galactopyranosyl acetate
(2R,3R,4R,5R)-3,4,6-Triacetyloxy-5-azidooxan-2-yl]methyl acetate
1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-D-galactopyranose, Min. 98% | [Molecular Formula]
C14H19N3O9 | [MDL Number]
MFCD02683262 | [MOL File]
84278-00-2.mol |
| Chemical Properties | Back Directory | [Melting point ]
113-114°C | [storage temp. ]
Hygroscopic, Refrigerator, Under Inert Atmosphere | [solubility ]
Chloroform (Slightly), Ethyl Acetate (Slightly) | [form ]
Solid | [color ]
White to Off-White | [BRN ]
4913077 |
| Hazard Information | Back Directory | [Chemical Properties]
White Crystalline Solid | [Uses]
D-Galactopyranose,2-azido-2-deoxy-,1,3,4,6-tetraacetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1]. | [reaction suitability]
reaction type: click chemistry | [References]
[1] Varki A, et al editors. Essentials of Glycobiology [Internet]. 4th ed. Cold Spring Harbor (NY): Cold Spring Harbor Laboratory Press; 2022. PMID:35536922 |
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