4-Deoxy-D-chitobioseheptaacetate

4-Deoxy-D-chitobiose heptaacetate 4-Deoxy-|A-D-chitobiose Peracetate is a unique chemical compound that has gained popularity in the scientific community due to its potential implications in various fields of research and industry. This paper aims to provide a comprehensive overview of this compound, including its definition, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions. Definition and Background 4-Deoxy-|A-D-chitobiose Peracetate, also known as 2-acetamido-2-deoxy-4,6-di-O-acetyl-hexopyranose, is a monosaccharide derivative that belongs to the family of N-acetylhexosamines. This compound was first synthesized in 1964 by Liotta and coworkers, and since then, it has gained attention due to its unusual structure and potential applications in various fields, including biotechnology, pharmaceuticals, and materials science. Synthesis and Characterization The synthesis of 4-Deoxy-|A-D-chitobiose Peracetate involves the reaction between 4-amino-4,6-dideoxyhexose and acetic anhydride under mild acidic conditions. This reaction leads to the formation of a white crystalline solid that can be purified by recrystallization. The characterization of this compound can be done using various analytical techniques such as NMR spectroscopy, IR spectroscopy, and mass spectrometry. Analytical Methods The characterization of 4-Deoxy-|A-D-chitobiose Peracetate can be done using various analytical methods such as NMR spectroscopy, IR spectroscopy, and mass spectrometry. NMR spectroscopy is the most common technique used for the structural elucidation of this compound. IR spectroscopy is used to identify the functional groups present in this compound, while mass spectrometry is used to determine its molecular weight. Biological Properties Several studies have investigated the biological properties of 4-Deoxy-|A-D-chitobiose Peracetate. It has been reported to have antimicrobial activity against various bacterial strains such as Escherichia coli and Staphylococcus aureus . This compound has also been shown to inhibit the proliferation of cancer cells in vitro and in vivo. Toxicity and Safety in Scientific Experiments Limited studies have been conducted to investigate the toxicity and safety of 4-Deoxy-|A-D-chitobiose Peracetate in scientific experiments. However, it has been reported to be non-toxic to mammalian cells at low concentrations. Applications in Scientific Experiments 4-Deoxy-|A-D-chitobiose Peracetate has various applications in scientific experiments. It is commonly used as a reagent for the synthesis of glycopeptides and glycolipids. This compound can also be used as a biomaterial for tissue engineering and drug delivery. Current State of Research The current state of research on 4-Deoxy-|A-D-chitobiose Peracetate is focused on elucidating its structure-function relationships and exploring its potential applications in various fields such as drug delivery, biotechnology, and materials science. Potential Implications in Various Fields of Research and Industry 4-Deoxy-|A-D-chitobiose Peracetate has potential implications in various fields of research and industry. In drug delivery, it can be used as a carrier for delivering drugs to specific tissues or cells. In biotechnology, it can be used as a biomaterial for tissue engineering and regenerative medicine. In materials science, it can be used for the development of new materials with unique properties. Limitations and Future Directions The main limitation of 4-Deoxy-|A-D-chitobiose Peracetate is its limited solubility in aqueous solutions, which restricts its use in certain applications. Future research directions should focus on overcoming this limitation and exploring new applications of this compound in various fields. Possible future directions include the development of new synthetic routes for producing this compound, the optimization of its solubility, and the investigation of its potential applications in nanotechnology and catalysis. Conclusion In conclusion, 4-Deoxy-|A-D-chitobiose Peracetate is a unique chemical compound with potential implications in various fields of research and industry. This paper has provided a comprehensive overview of this compound, including its definition, physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions. Further research is needed to explore the full potential of this compound and its implications in various fields of research and industry. CAS Number 1228931-51-8 Product Name 4-Deoxy-|A-D-chitobiose Peracetate IUPAC Name [(2S,4S,5R,6S)-5-acetamido-6-[(2R,3S,4R,5R,6S)-5-acetamido-4,6-diacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxy-4-acetyloxyoxan-2-yl]methyl acetate Molecular Formula C26H38N2O15 Molecular Weight 618.58 InChI InChI=1S/C26H38N2O15/c1-11(29)27-21-19(38-15(5)33)8-18(9-36-13(3)31)41-25(21)43-23-20(10-37-14(4)32)42-26(40-17(7)35)22(28-12(2)30)24(23)39-16(6)34/h18-26H,8-10H2,1-7H3,(H,27,29)(H,28,30)/t18-,19-,20+,21+,22+,23+,24+,25-,26+/m0/s1 InChI Key CBPIQIXAEQMDPR-ZKCIHQBLSA-N SMILES CC(=O)NC1C(CC(OC1OC2C(OC(C(C2OC(=O)C)NC(=O)C)OC(=O)C)COC(=O)C)COC(=O)C)OC(=O)C