71772-35-5
Chemical Structure
Methyl 6-deoxy-3,4-O-(1-methylethylidene)-α-D-galactopyranoside
- CAS No.: 71772-35-5
- Formula:C10H18O5
- Molecular Weight:218.25
IUPAC Name: (3aS,4R,6S,7R,7aR)-6-methoxy-2,2,4-trimethyltetrahydro-4H-[1,3]dioxolo[4,5-c]pyran-7-ol
InChIKey: UONDNTMXANWPHZ-ZEBDFXRSSA-N
SMILES: O[C@@H]1[C@]2([H])[C@](OC(C)(O2)C)([H])[C@H](O[C@@H]1OC)C
Biological Activity: Methyl 6-deoxy-3,4-O-(1-methylethylidene)-α-D-galactopyranoside 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 6-deoxy-3,4-O-(1-methylethylidene)-α-D-galactopyranoside | Methyl 6-deoxy-3,4-O-(1-methylethylidene)-α-D-galactopyranoside 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...
/
|
|||||||||||||||||||||||