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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
冷冻-20℃
- 保质期：
咨询
- 英文名：
4-Methoxyphenyl 2,3,4,6-tetra-O-acetyl-b-D-glucopyranoside
- 库存：
100+
- 供应商：
上海维亦特生物科技有限公司
- CAS号：
14581-81-8
14581-81-8
分子式：C21H26O11
分子量：454.42
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文献和实验Synthesis of Azido-Functionalized Carbohydrates for the Design of Glycoconjugates
of the carbohydrate derivative, or attached to a spacer arm. We describe here the syntheses of 2,3,4,6-tetra-O -acetyl-β-d -glucopyranosyl azide as well as 1-azido-3,6-dioxaoct-8-yl 2,3,4,6-tetra-O -acetyl-β-d -galactopyranoside and 1-azido-3,6-dioxaoct-8-yl
Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
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
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