38982-56-8
Chemical Structure
α-D-Galactopyranoside,methyl 6-O-(triphenylmethyl)-,triacetate
- CAS No.: 38982-56-8
- Formula:C32H34O9
- Molecular Weight:562.61
IUPAC Name: (2S,3R,4S,5S,6R)-2-methoxy-6-((trityloxy)methyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: CEIHIENXWVDRTC-NBCLCUQJSA-N
SMILES: CC(O[C@H]([C@@H]([C@H]([C@H](O1)OC)OC(C)=O)OC(C)=O)[C@H]1COC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)=O
Biological Activity: α-D-Galactopyranoside,methyl 6-O-(triphenylmethyl)-,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-Galactopyranoside,methyl 6-O-(triphenylmethyl)-,triacetate | α-D-Galactopyranoside,methyl 6-O-(triphenylmethyl)-,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...
/
|
|||||||||||||||||||||||
