| Identification | Back Directory | [Name]
BENZYL 2,3-O-ISOPROPYLIDENE-6-O-TRITYL-5-KETO-ALPHA-D-MANNOFURANOSE | [CAS]
91364-12-4 | [Synonyms]
Benzyl 2,3-O-isopropylidene-α-D-lyxo-hexofuranosid-5-ulose
Benzyl 2,3-O-Isopropylidene-6-O-trityl-5-keto-α-D-mannofuranose
BENZYL 2,3-O-ISOPROPYLIDENE-6-O-TRITYL-5-KETO-ALPHA-D-MANNOFURANOSE
PhenylMethyl-2,3-O-(1-Methylethylidene)-6-O-(triphenylMethyl)-α-D-lyxo-Hexofuranosid-5-ulose
α-D-lyxo-Hexofuranosid-5-ulose, phenylmethyl 2,3-O-(1-methylethylidene)-6-O-(triphenylmethyl)- | [Molecular Formula]
C35H34O6 | [MDL Number]
MFCD09750722 | [MOL File]
91364-12-4.mol | [Molecular Weight]
550.65 |
| Chemical Properties | Back Directory | [Boiling point ]
662.7±55.0 °C(Predicted) | [density ]
1.25±0.1 g/cm3(Predicted) | [solubility ]
soluble in Chloroform, Dichloromethane, Ethyl Acetate | [form ]
Solid | [color ]
White |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Benzyl 2,3-O-Isopropylidene-6-O-trityl-5-keto-α-D-mannofuranose 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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