| Identification | Back Directory | [Name]
2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE | [CAS]
29847-23-2 | [Synonyms]
2-Acetamido-2-deoxy--D-glucopyranosyl Azide
2-Acetamido-2-deoxy-2-D-glucopyranosyl Azide
2-Acetamido-2-deoxy-β-D-glucopyranosyl azide
2-ACETAMIDO-2-DEOXY-B-D-GLUCOPYRANOSYL AZIDE
2-ACETAMIDO-2-DEOXY-SS-D-GLUCOPYRANOSYL AZIDE
2-ACETAMIDO-2-DIDEOXY-B-D-GLUCOPYRANOSYL AZIDE
2-ACETAMIDO-2-DEOXY-BETA-D-GLUCOPYRANOSYL AZIDE
2-(Acetylamino)-2-deoxy--D-glucopyranosyl Azide
2-(Acetylamino)-2-deoxy-b-D-glucopyranosyl Azide
2-acetamido-1-azido-1-2-dideoxy-B-D-*glucopyranos
2-Acetamido-2-deoxy-β-D-glucopyranosyl azide ,98%
2-Acetamido-1-azido-1,2-dideoxy-β-D-glucopyranose
2-ACETAMIDO-1-AZIDO-1-2-DIDEOXY-B-D-GLUC OPYRANOSE
2-ACETAMIDO-1,2-DIDEOXY-BETA-D-GLUCOPYRANOSYL AZIDE
2-acetamido-1-azido-1,2-dideoxy-beta-D-glucopyranose
N-[2-AZIDO-4,5-DIHYDROXY-6-(HYDROXYMETHYL)OXAN-3-YL]ACETAMIDE | [Molecular Formula]
C8H14N4O5 | [MDL Number]
MFCD00049240 | [MOL File]
29847-23-2.mol | [Molecular Weight]
246.22 |
| Chemical Properties | Back Directory | [Melting point ]
142 °C (decomp) | [storage temp. ]
-20°C | [solubility ]
Methanol (Slightly), Water (Slightly) | [form ]
Solid | [color ]
White to Off-White | [Optical Rotation]
[α]/D -24.5±1.5°, c = 1 in H2O | [Stability:]
Hygroscopic | [InChI]
1S/C8H14N4O5/c1-3(14)10-5-7(16)6(15)4(2-13)17-8(5)11-12-9/h4-8,13,15-16H,2H2,1H3,(H,10,14)/t4-,5-,6-,7-,8-/m1/s1 | [InChIKey]
CCZCDCDASZJFGK-FMDGEEDCSA-N | [SMILES]
CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1N=[N+]=[N-] |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
2-Acetamido-2-deoxy-β-D-glucopyranosyl azide 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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