52260-48-7
Chemical Structure
Methyl 3-O-methyl-4,6-O-(phenylmethylene)-α-D-mannopyranoside
- CAS No.: 52260-48-7
- Formula:C15H20O6
- Molecular Weight:296.32
IUPAC Name: (4aR,6S,7S,8R,8aR)-6,8-dimethoxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-ol
InChIKey: KCXVHILKGUDBTH-UISBESDSSA-N
SMILES: CO[C@H]1[C@@]2([H])[C@](COC(C3=CC=CC=C3)O2)([H])O[C@@H]([C@H]1O)OC
Biological Activity: Methyl 3-O-methyl-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].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Methyl 3-O-methyl-4,6-O-(phenylmethylene)-α-D-mannopyranoside | Methyl 3-O-methyl-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. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
