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  • 30608-02-7 , 2,4-O-苄叉-L-木糖, 2,4-O-Benzylidene-L-xylose, CAS:30608-02-7
30608-02-7 , 2,4-O-苄叉-L-木糖, 2,4-O-Benzylidene-L-xylose, CAS:30608-02-7

30608-02-7 , 2,4-O-苄叉-L-木糖, 2,4-O-Benzylidene-L-xylose, CAS:30608-02-7

30608-02-7 , 2,4-O-苄叉-L-木糖,
2,4-O-Benzylidene-L-xylose,
CAS:30608-02-7
C12H14O5 / 238.24
MFCD00270488

2,4-O-Benzylidene-L-xylose

2,4-O-苄叉-L-木糖,

2,4-O-Benzylidene-L-xylose is a white crystalline powder with a melting point of about 125°C. It is an acetate salt that can be used in the synthesis of many natural products. It has been shown to inhibit HMG-CoA reductase and is used in the treatment of hypercholesterolemia. The reaction mechanism for this compound is not well understood, but it is believed to involve an acid catalyst and an organic solvent. The yield for this compound is low and it requires a long reaction time due to its high reactivity.

2,4-O-Benzylidene-L-xylose is a sugar derivative with a benzylidene group added to the xylose molecule. It has been extensively studied for its potential applications in various industries, including pharmaceuticals, cosmetics, and food. This compound is also known for its unique physical and chemical properties, making it a fascinating subject for scientific research.

Synthesis and Characterization

2,4-O-Benzylidene-L-xylose can be synthesized through the reaction of xylose with benzaldehyde in the presence of a catalyst. Various catalysts have been used for this reaction, including aluminum chloride, p-toluenesulfonic acid, and sodium hydroxide. The product can be characterized using analytical methods such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry.

Analytical Methods

NMR spectroscopy is a powerful technique for analyzing the structure of organic compounds. It can provide information about the number and type of atoms in a molecule, as well as their chemical environment. Mass spectrometry is another useful tool for identifying and characterizing organic compounds. It can provide information about the molecular weight and fragmentation pattern of a compound.

Biological Properties

2,4-O-Benzylidene-L-xylose has been shown to have antifungal and antibacterial properties, making it a potential candidate for use in the development of new drugs. It has also been studied for its potential as a glucose-lowering agent in the treatment of diabetes.

Toxicity and Safety in Scientific Experiments

Several studies have reported the safety of 2,4-O-Benzylidene-L-xylose in scientific experiments. It has been shown to have low toxicity and no adverse effects on animals.

Applications in Scientific Experiments

2,4-O-Benzylidene-L-xylose has been used in various scientific experiments, particularly in the field of organic chemistry. It has been utilized in the synthesis of various compounds, including cyclitols, glycosides, and iminosugars.

Current State of Research

Research on 2,4-O-Benzylidene-L-xylose is ongoing, particularly in the field of drug development. It is currently being investigated for its potential as an antifungal and antibacterial agent, as well as its ability to lower blood glucose levels.

Potential Implications in Various Fields of Research and Industry

The potential implications of 2,4-O-Benzylidene-L-xylose are vast and include its use in the development of new drugs, particularly in the treatment of fungal and bacterial infections, and in the treatment of diabetes. It may also have applications in the cosmetic and food industries.

Limitations and Future Directions

One limitation of 2,4-O-Benzylidene-L-xylose is its limited solubility in non-polar solvents, which may impact its potential use in certain applications. Future research should focus on developing new methods to improve its solubility and increasing its potential applications. Further research is also needed to fully understand its mechanism of action and potential side effects.

Future Directions

1. Investigating the potential of 2,4-O-Benzylidene-L-xylose as an anticancer agent

2. Developing new methods for improving its solubility in non-polar solvents

3. Investigating its potential as a food preservative

4. Developing new synthetic methods for 2,4-O-Benzylidene-L-xylose

5. Studying its potential as a chiral auxiliary in organic synthesis

6. Investigating its mode of action as an antifungal and antibacterial agent

7. Studying its potential as a coating material for medical devices

8. Investigating its potential as a drug delivery system

9. Developing new analytical methods for identifying and characterizing 2,4-O-Benzylidene-L-xylose

10. Studying its potential use as a potential anti-inflammatory agent.

CAS Number30608-02-7
Product Name2,4-O-Benzylidene-L-xylose
IUPAC Name(4S,5R,6S)-5-hydroxy-6-(hydroxymethyl)-2-phenyl-1,3-dioxane-4-carbaldehyde
Molecular FormulaC12H14O5
Molecular Weight238.24 g/mol
InChIInChI=1S/C12H14O5/c13-6-9-11(15)10(7-14)17-12(16-9)8-4-2-1-3-5-8/h1-6,9-12,14-15H,7H2/t9-,10+,11+,12?/m1/s1
InChI KeyMLCKHSIBLXIZKN-FEZOTEKNSA-N
SMILESC1=CC=C(C=C1)C2OC(C(C(O2)C=O)O)CO
Canonical SMILESC1=CC=C(C=C1)C2OC(C(C(O2)C=O)O)CO
Isomeric SMILESC1=CC=C(C=C1)C2O[C@H]([C@H]([C@H](O2)C=O)O)CO


CAS No: 30608-02-7 MDL No: MFCD00270488 Chemical Formula: C12H14O5 Molecular Weight: 238.24
References: 1. Kuszmann J, Podanyi B,, Carbohyd. Res., 1992, 225, 2, p247


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