150607-94-6
Chemical Structure
β-D-Glucopyranuronic acid,methyl ester,1,2,3,4-tetrakis(2-methylpropanoate)
- CAS No.: 150607-94-6
- Formula:C23H36O11
- Molecular Weight:488.53
IUPAC Name: (2S,3R,4S,5S,6S)-6-(methoxycarbonyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetrakis(2-methylpropanoate)
InChIKey: RFMOIPHVGPMCMF-RLAOKGOQSA-N
SMILES: CC(C)C(O[C@@H]1[C@H]([C@@H](O[C@@H]([C@H]1OC(C(C)C)=O)C(OC)=O)OC(C(C)C)=O)OC(C(C)C)=O)=O
Biological Activity: β-D-Glucopyranuronic acid,methyl ester,1,2,3,4-tetrakis(2-methylpropanoate) 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 | |||||||||||||||||||
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β-D-Glucopyranuronic acid,methyl ester,1,2,3,4-tetrakis(2-methylpropanoate) | 98.10% | β-D-Glucopyranuronic acid,methyl ester,1,2,3,4-tetrakis(2-methylpropanoate) 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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