| Identification | Back Directory | [Name]
ALLYL-ALPHA-D-MANNOPYRANOSIDE | [CAS]
41308-76-3 | [Synonyms]
Allyl α-D-mannopyranoside
Allyl a-D-mannopyranoside
Allyl α-D-mannopyranoside
ALLYL-ALPHA-D-MANNOPYRANOSIDE
2-Propenyl α-D-mannopyranoside
Allyl alpha-D-mannopyranoside 95%
2-Propenyl-alpha-D-mannopyranoside
α-D-Mannopyranoside, 2-propen-1-yl
a-D-Mannopyranoside, 2-propen-1-yl
α-D-Mannopyranoside, 2-propen-1-yl
(2R,3S,4S,5S,6S)-2-(HYDROXYMETHYL)-6-(PROP-2-EN-1-YLOXY)OXANE-3,4,5-TRIOL
(2S,3S,4S,5S,6R)-2-(Allyloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol | [Molecular Formula]
C9H16O6 | [MDL Number]
MFCD08274515 | [MOL File]
41308-76-3.mol | [Molecular Weight]
220.22 |
| Chemical Properties | Back Directory | [Melting point ]
94-100°C | [Boiling point ]
415.0±45.0 °C(Predicted) | [density ]
1.37±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [form ]
solid | [pka]
13.01±0.70(Predicted) |
| Hazard Information | Back Directory | [Uses]
Allyl α-D-mannopyranoside 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]. | [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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