37002-45-2
Chemical Structure
(-)-1,4-Di-O-tosyl-2,3-O-isopropylidene-L-threitol
- CAS No.: 37002-45-2
- Formula:C21H26O8S2
- Molecular Weight:470.56
IUPAC Name: ((4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate)
InChIKey: KPFDKWNWYAXRNJ-PMACEKPBSA-N
SMILES: O=S(OC[C@H]1[C@@H](OC(C)(O1)C)COS(=O)(C2=CC=C(C=C2)C)=O)(C3=CC=C(C=C3)C)=O
Biological Activity: (-)-1,4-Di-O-tosyl-2,3-O-isopropylidene-L-threitol 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 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
(-)-1,4-Di-O-tosyl-2,3-O-isopropylidene-L-threitol | (-)-1,4-Di-O-tosyl-2,3-O-isopropylidene-L-threitol 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...
/
|
|||||||||||||||||||||||
