53821-66-2
Chemical Structure
3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-tosyl-α-L-sorbose
- CAS No.: 53821-66-2
- Formula:C20H26O10S
- Molecular Weight:458.48
IUPAC Name: (5S,8S,9S,10S)-2,2-dimethyl-8-(tosyloxy)-1,3,6-trioxaspiro[4.5]decane-9,10-diyl diacetate
InChIKey: MJMXIHAIFBPIKU-DMUMMCEESA-N
SMILES: CC(O[C@@H]1[C@@]2(OC[C@@H]([C@H]1OC(C)=O)OS(=O)(C3=CC=C(C=C3)C)=O)OC(C)(OC2)C)=O
Biological Activity: 3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-tosyl-α-L-sorbose 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].
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3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-tosyl-α-L-sorbose | 3,4-Di-O-acetyl-1,2-O-isopropylidene-5-O-tosyl-α-L-sorbose 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. | |||||||||||||||||||||
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