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- 英文名：
2,3-Di-O-acetyl-4,6-O-benzylidene-N-Cbz-1-deoxynojirimycin
- CAS号：
2124269-54-9
2,3-Di-O-acetyl-4,6-O-benzylidene-N-Cbz-1-deoxynojirimycin
2124269-54-9
纯度：≥97%[1H-NMR]
分子式：C25H27NO8
分子量：469.48
储存：Store at 0 to -20 °C.
性状：White Amorphous Solid
溶剂：DMSO, DMF, DCM, EtOAc
别名：N-Benzyloxycarbonyl-4,6-O-phenylmethylene DNJ 2,3-diacetate, (4aR,7S,8R,8aR)-7,8-bis(Acetyloxy)hexahydro-2-phenyl-5H-1,3-dioxino[5,4-b]pyridine-5-carboxylic acid phenylmethyl ester
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文献和实验Enantioseparations in Nonaqueous Capillary Electrophoresis Using Charged Cyclodextrins
describes how to separate the enantiomers of three basic substances selected as model compounds, i.e., alprenolol, bupranolol, and terbutaline, using the negatively charged heptakis(2,3-di-O -acetyl-6-O -sulfo)-β-CD. The enantiomers of three acidic drugs
Characterization of Glycosaminoglycans by Capillary Electrophoresis
to a D-glucosamine (either N -sulfo or N -acetyl-d -glucosamine) residue. Both saccharide residues can be O -sulfonated at a variety of different positions, making these glycosaminoglycans structurally complex. Hyaluronic acid contains a simple repeating
Establishment of Stable Transfectant of CHO Lec Cells
Purpose and Backgrounds CHO lec 3.2.8.1 cells CHO Lec 3.2.8.1 cells have four independent mutations in the N- and O- glycosylation pathways (Stanley, 1989). N-linked carbohydrates produced by CHO Lec 3.2.8.1 cells are all of the high
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