| Identification | Back Directory | [Name]
Methyl 4,6-O-Benzylidene-2-deoxy-alpha-D-erythro-hexopyranosid-3-ulose Oxime | [CAS]
63598-32-3 | [Synonyms]
Methyl 4,6-O-Benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose Oxime
Methyl 4,6-O-Benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose Oxime
Methyl4,6-O-Benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-uloseOxime>
Methyl 4,6-O-Benzylidene-2-deoxy-alpha-D-erythro-hexopyranosid-3-ulose Oxime
α-D-erythro-Hexopyranosid-3-ulose, methyl 2-deoxy-4,6-O-(phenylmethylene)-, oxime, (R)- (9CI)
(NZ)-N-[(4aS,6S,8aS)-6-methoxy-2-phenyl-4a,6,7,8a-tetrahydro-4H-pyrano[3,2-d][1,3]dioxin-8-ylidene]hydroxylamine | [Molecular Formula]
C14H17NO5 | [MOL File]
63598-32-3.mol | [Molecular Weight]
279.29 |
| Chemical Properties | Back Directory | [Melting point ]
198.0 to 202.0 °C | [Boiling point ]
454.8±45.0 °C(Predicted) | [density ]
1.39±0.1 g/cm3(Predicted) | [form ]
powder to crystal | [pka]
10.85±0.60(Predicted) | [color ]
White to Almost white |
| Hazard Information | Back Directory | [Uses]
Methyl 4, 6-O-Benzylidene-2-deoxy-α-d-Erythro-Hexopyranosid-3-ulose oxime is a class of biochemical reagents used in the study of glycobiology. 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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