2,3,4,6-Tetra-O-acetyl-a-D-mannopyranosyl chloride ,
四乙酰基-α-D-氯代甘露糖 ,
CAS:14257-40-0
C14H19ClO9 / 366.75
MFCD00067355
2,3,4,6-四乙酰基-α-D-氯代甘露糖
Acetochloro-alpha-D-mannose is a chemical compound, also known as ACM, which is a member of the mannose family. It is a white crystalline substance that is soluble in water and can be synthesized in the laboratory. This compound is widely used in various scientific experiments, especially in the field of biochemistry.
Synthesis and Characterization:
The synthesis of ACM is usually carried out from L-mannose, which is then chlorinated and acetylated. The synthesized ACM is then purified using chromatographic methods. The characterization of ACM is done using various techniques, including nuclear magnetic resonance (NMR) spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, and mass spectrometry.
Analytical Methods:
ACM can be analyzed using various analytical methods, including high-performance liquid chromatography (HPLC), gas chromatography (GC), and liquid chromatography-mass spectrometry (LC-MS). These techniques are widely used for the identification and quantification of ACM in different experimental samples.
Biological Properties:
ACM has been reported to possess various biological properties, including its ability to inhibit bacterial growth, regulate immune responses, and modulate cell adhesion. It has also been reported to have antiviral and antitumor activities.
Toxicity and Safety in Scientific Experiments:
Several studies have reported the toxic effects of ACM on different cell lines and animal models. The compound has been reported to cause toxicity to liver and kidney tissues, as well as exhibit mutagenic and carcinogenic effects. Therefore, the use of ACM in scientific experiments requires strict safety protocols and guidelines.
Applications in Scientific Experiments:
ACM has a wide range of applications in scientific experiments, including the production of pharmaceuticals, development of biomaterials, and biosynthesis of glycans. It has also been used as a tool for studying the role of glycosyltransferases in regulating cellular processes.
Current State of Research:
Current research on ACM is focused on understanding its biological activities and exploring its potential applications in different fields of research. Studies are being conducted to develop novel drugs and therapies based on ACM as a lead compound.
Potential Implications in Various Fields of Research and Industry:
ACM has the potential to revolutionize various fields of research and industry, including drug discovery, biotechnology, and materials science. It can be used as a lead compound for the development of novel drugs, as well as for the design and synthesis of novel biomaterials.
Limitations and Future Directions:
One major limitation of using ACM in scientific experiments is its toxicity and safety concerns. Thus, researchers need to develop safer and more efficient synthetic methods of producing ACM. Future directions for research include exploring the use of ACM in other fields of research, such as agriculture and environmental science, as well as identifying new targets for drug discovery using ACM as a lead compound.
In conclusion, the study of Acetochloro-alpha-D-mannose is an important area of research in the field of biochemistry due to its wide range of biological activities and potential applications in various fields of research and industry. Further research is needed to understand its full potential and address its limitations in order to fully realize its impact on science and technology.
CAS Number | 14257-40-0 |
Product Name | Acetochloro-alpha-D-mannose |
IUPAC Name | [(2R,3R,4S,5S,6R)-3,4,5-triacetyloxy-6-chlorooxan-2-yl]methyl acetate |
Molecular Formula | C₁₄H₁₉ClO₉ |
Molecular Weight | 366.75 |
InChI | InChI=1S/C14H19ClO9/c1-6(16)20-5-10-11(21-7(2)17)12(22-8(3)18)13(14(15)24-10)23-9(4)19/h10-14H,5H2,1-4H3/t10-,11-,12+,13+,14+/m1/s1 |
SMILES | CC(=O)OCC1C(C(C(C(O1)Cl)OC(=O)C)OC(=O)C)OC(=O)C |
Synonyms | Acetochloro-α-D-mannose; α-D-Mannopyranosyl Chloride, 2,3,4,6-Tetraacetate; |
CAS No: 14257-40-0 Synonyms: 1-Chloro-2,3,4,6-tetra-O-acetyl-a-D-mannopyranosideAcetochloro-a-D-mannose MDL No: MFCD00067355 Chemical Formula: C14H19ClO9 Molecular Weight: 366.75 |
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