| Identification | Back Directory | [Name]
BENZYL 2,3-O-ISOPROPYLIDENE-ALPHA-D-MANNOFURANOSIDE | [CAS]
20689-03-6 | [Synonyms]
Benzyl 2,3-O-Isopropylidene-α-D-mannofuranoside
Benzyl 2-O,3-O-isopropylidene-α-D-mannofuranoside
PhenylMethyl 2,3-O-(1-Methylethylidene)-α-D-Mannofuranoside
Phenylmethyl 2,3-O-(1-methylethylidene)-α-D-mannofuranoside
Benzyl 2,3-O-isopropylidene-alpha-D-mannofuranoside min. 98%
α-D-Mannofuranoside, phenylmethyl 2,3-O-(1-methylethylidene)-
(1R)-1-((4R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)ethane-1,2-diol | [Molecular Formula]
C16H22O6 | [MDL Number]
MFCD02683277 | [MOL File]
20689-03-6.mol | [Molecular Weight]
310.34 |
| Chemical Properties | Back Directory | [Melting point ]
61-64°C | [storage temp. ]
-20°C Freezer | [solubility ]
Soluble in chloroform, dichloromethane or DMSO | [form ]
Powder | [color ]
White to Off-white |
| Hazard Information | Back Directory | [Chemical Properties]
White Solid | [Uses]
Phenylmethyl 2,3-O-(1-methylethylidene)-α-D-mannofuranoside 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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