3254-17-9
Chemical Structure
α-D-Glucopyranose,1,2-O-(1-ethoxyethylidene)-,3,4,6-triacetate
- CAS No.: 3254-17-9
- Formula:C16H24O10
- Molecular Weight:376.36
IUPAC Name: (3aR,5R,6R,7S,7aR)-5-(acetoxymethyl)-2-ethoxy-2-methyltetrahydro-5H-[1,3]dioxolo[4,5-b]pyran-6,7-diyl diacetate
InChIKey: ULBLUAFHNLHIND-VAZACWIESA-N
SMILES: CC(O[C@@H]1[C@]2([H])[C@](OC(C)(O2)OCC)([H])O[C@@H]([C@H]1OC(C)=O)COC(C)=O)=O
Biological Activity: α-D-Glucopyranose,1,2-O-(1-ethoxyethylidene)-,3,4,6-triacetate 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
α-D-Glucopyranose,1,2-O-(1-ethoxyethylidene)-,3,4,6-triacetate | α-D-Glucopyranose,1,2-O-(1-ethoxyethylidene)-,3,4,6-triacetate 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...
/
|
|||||||||||||||||||||||
