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  • 165524-85-6 , 6-O-苄基-D-葡萄糖烯, 6-O-Benzyl-D-glucal , CAS:165524-85-6
165524-85-6 , 6-O-苄基-D-葡萄糖烯, 6-O-Benzyl-D-glucal , CAS:165524-85-6

165524-85-6 , 6-O-苄基-D-葡萄糖烯, 6-O-Benzyl-D-glucal , CAS:165524-85-6

165524-85-6 ,6-O-苄基-D-葡萄糖烯,
6-O-Benzyl-D-glucal ,
CAS:165524-85-6
C13H16O4 / 236.26
MFCD04112728

6-O-Benzyl-D-glucal

6-O-苄基-D-葡萄糖烯,

6-O-Benzyl-D-glucal is a versatile chemical compound with numerous potential applications in various fields of research and industry. This paper aims to provide a comprehensive overview of 6-O-Benzyl-D-glucal by discussing its definition and background, 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.

Synthesis and Characterization

6-O-Benzyl-D-glucal can be synthesized by the benzylidenation of D-glucose using benzaldehyde in the presence of an acid catalyst. The resulting compound can be characterized using various analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and mass spectrometry.

Analytical Methods

NMR spectroscopy is a powerful technique for the structural characterization of 6-O-Benzyl-D-glucal. The technique allows for the determination of the molecular structure and chemical environment of each atom in the compound. IR spectroscopy can be used to identify functional groups present in the compound. Mass spectrometry can provide information about the molecular weight and fragmentation pattern of the compound.

Biological Properties

6-O-Benzyl-D-glucal has been shown to exhibit antibacterial, antifungal, and antiviral properties in vitro. The compound has also been found to inhibit the growth of cancer cells in cell culture studies. Further research is needed to understand the mechanisms of its biological activity and its potential as a therapeutic agent.

Toxicity and Safety in Scientific Experiments

6-O-Benzyl-D-glucal has a low toxicity profile and is generally considered safe for use in scientific experiments. However, caution should be exercised when handling the compound, as it can cause skin and eye irritation. Proper safety protocols, such as wearing protective clothing and gloves, should be followed when working with the compound.

Applications in Scientific Experiments

6-O-Benzyl-D-glucal has numerous potential applications in various fields of research and industry. It can be used in the synthesis of glycosides, which are important compounds in medicine and natural product research. It can also be used to create glycosylamines, which have applications in carbohydrate chemistry and physiology. Additionally, 6-O-Benzyl-D-glucal can be used to create glycosyl sulfones, which have applications in drug discovery.

Current State of Research

Limited research has been conducted on 6-O-Benzyl-D-glucal, and further research is needed to explore its potential applications and properties. The compound's antibacterial, antifungal, and antiviral properties have been established in vitro, but further research is needed to explore its potential therapeutic applications in vivo.

Potential Implications in Various Fields of Research and Industry

6-O-Benzyl-D-glucal has potential implications in various fields of research and industry, including medicinal chemistry, natural product research, carbohydrate chemistry, and drug discovery. It can be used to create glycosides, glycosylamines, and glycosyl sulfones, which have applications in these fields.

Limitations

One of the main limitations of 6-O-Benzyl-D-glucal is its low solubility in nonpolar solvents, which limits its potential applications in some fields. Additionally, little research has been conducted on the compound's biological activity in vivo, which limits our understanding of its potential therapeutic applications.

Future Directions

Numerous future directions are possible for research on 6-O-Benzyl-D-glucal, including:

1. Exploration of the compound's potential as a therapeutic agent in vivo.

2. Development of more efficient and environmentally friendly synthetic methods for the compound.

3. Exploration of the compound's potential applications in drug discovery.

4. Investigation of the compound's potential as an antibacterial, antifungal, and antiviral agent in vivo.

5. Exploration of the compound's potential applications in carbohydrate chemistry.

6. Studies on the compound's potential applications in natural product research.

7. Investigation of the compound's potential utility in nanotechnology.

8. Development of new analytical techniques to study the compound's properties and behavior.

9. Studies on the effect of different substituents on the compound's physical and chemical properties.

10. Exploration of the compound's potential applications in chiral synthesis and asymmetric catalysis.

Conclusion

6-O-Benzyl-D-glucal is a versatile chemical compound with numerous potential applications in various fields of research and industry. Further research is needed to explore its potential therapeutic applications, synthetic methods, properties, and biological activity in vivo. Through continued exploration and investigation, this compound has the potential to significantly impact the fields of chemistry, medicine, and materials science.

CAS Number165524-85-6
Product Name6-O-Benzyl-D-glucal
IUPAC Name(2R,3S,4R)-2-(phenylmethoxymethyl)-3,4-dihydro-2H-pyran-3,4-diol
Molecular FormulaC13H16O4
Molecular Weight236.26 g/mol
InChIInChI=1S/C13H16O4/c14-11-6-7-17-12(13(11)15)9-16-8-10-4-2-1-3-5-10/h1-7,11-15H,8-9H2/t11-,12-,13+/m1/s1
InChI KeyRHDGBCAJRWMYHR-UPJWGTAASA-N
SMILESC1=CC=C(C=C1)COCC2C(C(C=CO2)O)O
Canonical SMILESC1=CC=C(C=C1)COCC2C(C(C=CO2)O)O
Isomeric SMILESC1=CC=C(C=C1)COC[C@@H]2[C@H]([C@@H](C=CO2)O)O


CAS No: 165524-85-6 MDL No: MFCD04112728 Chemical Formula: C13H16O4 Molecular Weight: 236.26

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