D-glucopyranosepentabenzoate, CAS:3006-49-3

Glucopyranose pentabenzoate is a chemical compound used in various scientific experiments in fields such as pharmaceuticals, material sciences, and nanotechnology. It is synthesized through the reaction of glucose with benzyl chloride, followed by the substitution of hydroxyl groups with benzoate groups. In this paper, we will explore the definition, properties, synthesis, 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 of glucopyranose pentabenzoate. Synthesis and Characterization Glucopyranose pentabenzoate is synthesized through the reaction of glucose with benzyl chloride, followed by the substitution of hydroxyl groups with benzoate groups. The reaction is carried out in the presence of a base, such as sodium hydroxide or potassium hydroxide, and a solvent, such as dimethyl sulfoxide or ethyl acetate. The product is then purified through recrystallization and characterized through various analytical methods, such as Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR) spectroscopy, and high-performance liquid chromatography (HPLC). Analytical Methods Various analytical methods are used to characterize and quantify glucopyranose pentabenzoate. FTIR spectroscopy is used to identify functional groups present in the compound, and NMR spectroscopy is used to determine the molecular structure and purity. HPLC is used to separate and quantify the compound in mixtures. Biological Properties Glucopyranose pentabenzoate has been shown to exhibit biological properties such as antiviral, anti-inflammatory, and antioxidant activities. It has also been used as a carrier for delivering drugs to target cells or tissues. Toxicity and Safety in Scientific Experiments Studies have shown that glucopyranose pentabenzoate is relatively safe and non-toxic in scientific experiments. However, proper precautions should be taken, such as wearing gloves and protective clothing, to prevent contact with skin or inhalation. Applications in Scientific Experiments Glucopyranose pentabenzoate is a versatile compound with various applications in scientific experiments. It is used as a starting material for the synthesis of surfactants, polymers, and dendrimers. It is also used as a carrier for delivering drugs to target cells or tissues. Current State of Research Research on glucopyranose pentabenzoate is still ongoing, with many researchers exploring its potential applications in various fields. Recent studies have focused on its use as a scaffold for tissue engineering and as a biomaterial for drug delivery. Potential Implications in Various Fields of Research and Industry Glucopyranose pentabenzoate has promising implications in various fields of research and industry. In the field of material sciences, it can be used as a starting material for the synthesis of polymers, surfactants, and dendrimers. In the field of pharmaceuticals, it can be used as a carrier for delivering drugs to target cells or tissues. In the field of nanotechnology, it can be used as a scaffold for tissue engineering. Limitations and Future Directions One major limitation of glucopyranose pentabenzoate is its low solubility in water, which limits its use in certain applications. Future research should focus on developing derivatives of glucopyranose pentabenzoate with improved solubility in water. Additionally, more research is needed to investigate its potential as a biomaterial for tissue engineering and drug delivery. Future Directions - Development of glucopyranose pentabenzoate derivatives with improved solubility in water - Investigation of its potential as a biomaterial for tissue engineering and drug delivery - Exploration of its use as a surfactant in various applications - Investigation of its potential as a photovoltaic material - Investigation of its potential as an antibacterial agent - Development of glucopyranose pentabenzoate-based nanoparticles for targeted drug delivery - Investigation of its potential as a membrane material for separation processes - Exploration of its use as a coating material in the food industry - Development of glucopyranose pentabenzoate-based hydrogels for biomedical applications - Investigation of its potential as a catalyst for organic reactions. CAS Number 3006-49-3 Product Name Glucopyranose pentabenzoate IUPAC Name [(2R,3R,4S,5R)-3,4,5,6-tetrabenzoyloxyoxan-2-yl]methyl benzoate Molecular Formula C41H32O11 Molecular Weight 700.69 g/mol InChI InChI=1S/C41H32O11/c42-36(27-16-6-1-7-17-27)47-26-32-33(49-37(43)28-18-8-2-9-19-28)34(50-38(44)29-20-10-3-11-21-29)35(51-39(45)30-22-12-4-13-23-30)41(48-32)52-40(46)31-24-14-5-15-25-31/h1-25,32-35,41H,26H2/t32-,33-,34+,35-,41?/m1/s1 InChI Key JJNMLNFZFGSWQR-XBHBEMSESA-N SMILES C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6 Synonyms D-Glucopyranose 1,2,3,4,6-Pentabenzoate; Canonical SMILES C1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6 Isomeric SMILES C1=CC=C(C=C1)C(=O)OC[C@@H]2[C@H]([C@@H]([C@H](C(O2)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6 CAS No: 3006-49-3 Synonyms: D-Glucopyranose 1,2,3,4,6-pentabenzoate Chemical Formula: C41H32O11 Molecular Weight: 700.69