Identification | Back Directory | [Name]
Allyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy--D-glucopyranoside | [CAS]
28738-44-5 | [Synonyms]
Allyl 2-Acetamido-2-deoxy--D-glucopyranoside 3,4,6-Triacetate Allyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy--D-glucopyranoside Allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside Allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-beta-D-glucopyranoside 2-Propenyl 2-(Acetylamino)-2-deoxy--D-glucopyranoside 3,4,6-Triacetate | [EINECS(EC#)]
1533716-785-6 | [Molecular Formula]
C17H25NO9 | [MDL Number]
MFCD12407871 | [MOL File]
28738-44-5.mol | [Molecular Weight]
387.39 |
Chemical Properties | Back Directory | [Appearance]
White Solid | [Melting point ]
151-157°C (dec.) | [Boiling point ]
531.3±50.0 °C(Predicted) | [density ]
1.23±0.1 g/cm3(Predicted) | [storage temp. ]
Refrigerator | [solubility ]
Soluble in Methanol | [form ]
Solid | [pka]
13.67±0.70(Predicted) | [color ]
WhiteOff-White |
Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Allyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 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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