| Identification | Back Directory | [Name]
4-METHOXYPHENYL 3,4,6-TRI-O-ACETYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE | [CAS]
138906-41-9 | [Synonyms]
4-Methoxyphenyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-&beta
4-Methoxyphenyl 3,4,6-Tri-O-cetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside
4-Methoxyphenyl3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-b-D-glucopyranoside
4-Methoxyphenyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
4-Methoxyphenyl 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
4-Methoxyphenyl3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranoside>
4-METHOXYPHENYL 3,4,6-TRI-O-ACETYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE
4-METHOXYPHENYL 3,4,6-TRI-O-ACETYL-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE USP/EP/BP
(2R,3S,4R,5R,6S)-2-(Acetoxymethyl)-5-(1,3-dioxoisoindolin-2-yl)-6-(4-methoxyphenoxy)tetrahydro-2H-pyran-3,4-diyl diacetate | [Molecular Formula]
C27H27NO11 | [MDL Number]
MFCD06797125 | [MOL File]
138906-41-9.mol | [Molecular Weight]
541.5 |
| Chemical Properties | Back Directory | [Melting point ]
149 °C | [Boiling point ]
656.8±55.0 °C(Predicted) | [density ]
1.40±0.1 g/cm3(Predicted) | [storage temp. ]
Freezer | [solubility ]
almost transparency in Chloroform | [form ]
powder to crystal | [pka]
-2.55±0.20(Predicted) | [color ]
White to Light yellow to Light orange |
| Hazard Information | Back Directory | [Uses]
4-Methoxyphenyl 3,4, 6-tri-o-acetyl-2-deoxy-2-phthalimido-β-d-Glucopyranoside (4-methoxyphenyl) 3,4, 6-tri-o-acetyl-2-deoxy-2-phthalimido-beta-d-Glucopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology[1]. | [References]
[1] Opdenakker G, Rudd PM, Ponting CP, Dwek RA. Concepts and principles of glycobiology. FASEB J. 1993 Nov;7(14):1330-7. DOI:10.1096/fasebj.7.14.8224606 |
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