| Identification | Back Directory | [Name]
Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside | [CAS]
62774-16-7 | [Synonyms]
1,3-Di-O-benzyl-4,6-O-benzylidene-a-D-mannopyranoside
Benzyl 3-O-Benzyl-4,6-O-benzylidene-a-D-mannopyranoside
Benzyl 3-O-Benzyl-4,6-O-benzylidene-α-D-mannopyranoside
Phenylmethyl 3-O-(Phenylmethyl)-4,6-O-(phenylmethylene))-α-D-mannopyranoside
Phenylmethyl 3-O-(Phenylmethyl)-4,6-O-(phenylmethylene))-a-D-mannopyranoside | [Molecular Formula]
C27H28O6 | [MDL Number]
MFCD09952135 | [MOL File]
62774-16-7.mol | [Molecular Weight]
448.51 |
| Hazard Information | Back Directory | [Chemical Properties]
Colorless Oil | [Uses]
Phenylmethyl 3-O-(phenylmethyl)-4,6-O-(phenylmethylene)-α-D-mannopyranoside 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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