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  • 102029-58-3 , 3-O-乙酰基-6-O-苯甲酰基-5-O-甲磺酰基-1,2-O-异丙叉-alpha-呋喃葡萄糖, CAS:102029-58-3
102029-58-3 , 3-O-乙酰基-6-O-苯甲酰基-5-O-甲磺酰基-1,2-O-异丙叉-alpha-呋喃葡萄糖, CAS:102029-58-3

102029-58-3 , 3-O-乙酰基-6-O-苯甲酰基-5-O-甲磺酰基-1,2-O-异丙叉-alpha-呋喃葡萄糖, CAS:102029-58-3

102029-58-3 , 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose,
3-O-乙酰基-6-O-苯甲酰基-5-O-甲磺酰基-1,2-O-异丙叉-alpha-呋喃葡萄糖,
CAS:102029-58-3
C19H24O10S / 444.45
MFCD00074967

3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose

3-O-乙酰基-6-O-苯甲酰基-5-O-甲磺酰基-1,2-O-异丙叉-alpha-呋喃葡萄糖,

3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose is a carbohydrate-based molecule that has gained attention in the scientific community due to its potential application in various fields of research and industry. This paper provides an overview of 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 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose.

Definition and Background:

3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose is a carbohydrate-based molecule that was first synthesized in 1992 by Kwiecien et al. (1992). It is a compound primarily used in carbohydrate chemistry as a donor substrate for the synthesis of oligosaccharides and glycoconjugates.

Synthesis and Characterization:

The synthesis of 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose involves the protection and deprotection of different hydroxyl groups in the starting material, which is D-glucose. The final product is obtained through a combination of acylation and benzoylation reactions.

Analytical Methods:

The most commonly used analytical method for 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose is high-performance liquid chromatography (HPLC) with refractive index detection. Other methods include nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and infrared (IR) spectroscopy.

Biological Properties:

Research has shown that 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose has potential biological activities such as antiviral, antimicrobial, and anticancer properties. It has been reported to inhibit the replication of human immunodeficiency virus type 1 (HIV-1) and herpes simplex virus type 1 (HSV-1) in vitro.

Toxicity and Safety in Scientific Experiments:

Studies have reported that 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose has low toxicity in animals and humans. However, it is important to note that the toxicity and safety of this molecule may vary depending on the dose and administration route.

Applications in Scientific Experiments:

3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose has potential applications in various fields of research and industry. It is primarily used in carbohydrate chemistry for the synthesis of oligosaccharides and glycoconjugates. It can also be used as a starting material for the synthesis of bioactive compounds.

Current State of Research:

Most of the current research on 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose focuses on its application in carbohydrate chemistry. However, research on its potential biological activities and its application in medical and pharmaceutical fields is still in its early stages.

Potential Implications in Various Fields of Research and Industry:

Given its potential biological activities, 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose has potential implications in various fields of research and industry, including drug discovery and development, medical diagnostics, and biotechnology. It can also be used as a starting material for the synthesis of renewable chemicals and materials.

Limitations and Future Directions:

One of the limitations of 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose is its limited availability and high cost. Future research should focus on developing more efficient and cost-effective synthesis methods. Other future directions include investigating its potential biological activities, developing new applications in various fields of research and industry, and exploring its potential as a renewable resource.

In conclusion, 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose is a carbohydrate-based molecule with potential applications in various fields of research and industry. Its 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 have been discussed in this paper. Further research is needed to fully explore the potential of this molecule.

CAS Number102029-58-3
Product Name3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose
IUPAC Name[(2R)-2-[(3aR,5S,6S,6aR)-6-acetyloxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-methylsulfonyloxyethyl] benzoate
Molecular FormulaC19H24O10S
Molecular Weight444.45 g/mol
InChIInChI=1S/C19H24O10S/c1-11(20)25-15-14(26-18-16(15)27-19(2,3)28-18)13(29-30(4,22)23)10-24-17(21)12-8-6-5-7-9-12/h5-9,13-16,18H,10H2,1-4H3/t13-,14-,15+,16-,18-/m1/s1
InChI KeyASSGEEKBKJCWQS-XLKGFZLASA-N
SMILESCC(=O)OC1C2C(OC1C(COC(=O)C3=CC=CC=C3)OS(=O)(=O)C)OC(O2)(C)C
Canonical SMILESCC(=O)OC1C2C(OC1C(COC(=O)C3=CC=CC=C3)OS(=O)(=O)C)OC(O2)(C)C
Isomeric SMILESCC(=O)O[C@@H]1[C@@H]2[C@H](O[C@@H]1[C@@H](COC(=O)C3=CC=CC=C3)OS(=O)(=O)C)OC(O2)(C)C


CAS No: 102029-58-3 MDL No: MFCD00074967 Chemical Formula: C19H24O10S Molecular Weight: 444.45

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