28528-86-1,6-氯-D-吡喃葡萄糖,
6-Chloro-D-glucose,
CAS:28528-86-1
C6H11ClO5 / 198.60
6-Chloro-6-deoxy-alpha-d-glucopyranose is a chemical compound with a molecular formula of C6H11ClO5. It is also known as 6-chloro-6-deoxy-alpha-d-glucopyranoside or 6-chloro-6-deoxyglucose. This compound is not commonly found in nature, but it is synthesized and used in a variety of scientific experiments. In this paper, we will discuss the 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, and limitations and future directions of 6-Chloro-6-deoxy-alpha-d-glucopyranose.
Definition and Background
6-Chloro-6-deoxy-alpha-d-glucopyranose is a synthetic chemical compound that is closely related to the naturally occurring glucose molecule. It is a monosaccharide, which means that it is a simple sugar that cannot be further hydrolyzed into a smaller unit. This compound is used in various scientific experiments as a precursor molecule for the synthesis of other compounds. The chloro group attached to the glucose molecule makes it useful in some specific applications.
Physical and Chemical Properties
The physical and chemical properties of 6-Chloro-6-deoxy-alpha-d-glucopyranose are crucial for its synthesis and applications. This compound is a white to off-white crystalline powder that is soluble in water and ethanol. The melting point of this compound ranges from 165-169℃. It is a stable compound when stored at room temperature and is not susceptible to oxidation or degradation.
Synthesis and Characterization
6-Chloro-6-deoxy-alpha-d-glucopyranose is synthesized using several different methods such as reductive chlorination of glucose, catalytic hydrogenation of 6-chlorosugar, and others. The synthesis process involves the use of several chemical reagents and catalysts. Characterization of the synthesized compound is done using various analytical techniques such as NMR, FT-IR, and Mass Spectrometry.
Analytical Methods
Several analytical methods are used to determine the purity and identity of 6-Chloro-6-deoxy-alpha-d-glucopyranose. These techniques include NMR (Nuclear Magnetic Resonance Spectroscopy), FT-IR (Fourier Transform Infrared Spectroscopy), HPLC (High-Performance Liquid Chromatography), and GC-MS (Gas Chromatography-Mass Spectrometry).
Biological Properties
There is little information available on the biological properties of 6-Chloro-6-deoxy-alpha-d-glucopyranose. However, some studies have shown that it exhibits some antiviral and antibacterial properties. Further research is required to explore its potential in biological applications.
Toxicity and Safety in Scientific Experiments
The safety of using 6-Chloro-6-deoxy-alpha-d-glucopyranose in scientific experiments is a crucial concern. It is recommended to use appropriate safety precautions when handling this compound due to its potential toxicity. It is also crucial to dispose of any waste products appropriately.
Applications in Scientific Experiments
6-Chloro-6-deoxy-alpha-d-glucopyranose is a valuable precursor molecule for the synthesis of various compounds such as synthetic building blocks, thiazoline, and C-nucleoside analogues. It is also used as a reagent for the determination of blood glucose levels in biochemical assays.
Current State of Research
There is significant research on the synthesis and characterization of 6-Chloro-6-deoxy-alpha-d-glucopyranose in recent years. Several studies have explored its potential applications in various fields of research.
Potential Implications in Various Fields of Research and Industry
6-Chloro-6-deoxy-alpha-d-glucopyranose has the potential to impact various fields of research and industry, including the pharmaceutical industry, biotechnology, and material science. Its ability to act as a precursor molecule for the synthesis of various compounds may lead to the development of new drugs, materials, and technologies.
Limitations and Future Directions
Despite the potential applications of 6-Chloro-6-deoxy-alpha-d-glucopyranose, there are some limitations, including its toxicity and the complexity of its synthesis. Further research is required to explore its potential applications fully. Future directions for research in this area include the development of alternative synthesis methods, exploration of its biological applications, and its application in material science.
Conclusion
6-Chloro-6-deoxy-alpha-d-glucopyranose is a synthetic compound that has the potential to impact various fields of research and industry. Its ability to act as a precursor molecule for the synthesis of various compounds makes it a valuable reagent in many scientific experiments. However, more research is necessary to explore its potential applications fully. Further exploration of its biological applications and alternative synthesis methods may lead to new developments in this area. While there are some limitations and concerns over its toxicity, 6-Chloro-6-deoxy-alpha-d-glucopyranose remains a valuable chemical compound in the world of scientific research.
CAS Number | 28528-86-1 |
Product Name | 6-Chloro-6-deoxy-alpha-d-glucopyranose |
IUPAC Name | (2S,3R,4S,5S,6S)-6-(chloromethyl)oxane-2,3,4,5-tetrol |
Molecular Formula | C6H11ClO5 |
Molecular Weight | 198.6 g/mol |
InChI | InChI=1S/C6H11ClO5/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-6,8-11H,1H2/t2-,3-,4+,5-,6+/m1/s1 |
InChI Key | QMWDIHPSUCUMFU-DVKNGEFBSA-N |
SMILES | C(C1C(C(C(C(O1)O)O)O)O)Cl |
Synonyms | (2S,3R,4S,5S,6S)-6-(Chloromethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol |
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