| Identification | Back Directory | [Name]
N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL | [CAS]
151963-95-0 | [Synonyms]
N-Benzyl-2,3,4,6-tetra-O-benzyl-1-deoxy-L-idonojiriMycin
N-BENZYL-2,3,4,6-TETRA-O-BENZYL-1,5-DIDEOXY-IMINO-L-IDITOL
(2S,3R,4R,5S)-3,4,5-Tris(phenylMethoxy)-2-[(phenylMethoxy)Methyl]-1-(phenylMethyl)piperidine | [Molecular Formula]
C41H43NO4 | [MDL Number]
MFCD09840017 | [MOL File]
151963-95-0.mol | [Molecular Weight]
613.784 |
| Chemical Properties | Back Directory | [Appearance]
Yellow Oil | [Boiling point ]
695.6±55.0 °C(Predicted) | [density ]
1.18±0.1 g/cm3(Predicted) | [storage temp. ]
Refrigerator | [solubility ]
Acetone (Slightly), Chloroform (Slightly), DMSO (Slightly) | [form ]
Oil | [pka]
7.61±0.10(Predicted) | [color ]
Clear Yellow to Orange | [Stability:]
Moisture, Temperature Sensitive |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow Oil | [Uses]
N-Benzyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-imino-L-iditol 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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