28140-37-6 , 3,4,6-Tri-O-acetyl-1,2-O-(ethoxyethylidene)-b-D-mannopyranose,
3,4,6-O-三乙酰基-b-D-吡喃甘露糖-1,2-原酸乙酯,
CAS:28140-37-6
C16H24O10 / 376.36
MFCD01863564
3,4,6-O-三乙酰基-b-D-吡喃甘露糖-1,2-原酸乙酯,
3,4,6-Tri-O-acetyl-1,2-O-ethoxyethylidene-b-D-mannopyranose is a synthetic monosaccharide that is used as a substrate for the production of various oligosaccharides and polysaccharides. This substance can be fluorinated to produce 3,4,6-tri-O-(3′,5′ -difluoro) acetyl-1,2:5′,6′ -di(O—ethoxyethylidene)-b-D mannopyranose. It has been shown that methylation of the C1 position in this compound results in a variety of different compounds with different properties.
1,2-O-(1-Ethoxyethylidene)-beta-D-mannopyranose triacetate is a synthetic compound used for various scientific and industrial purposes. It is a derivative of D-mannose and is formed by the reaction of D-mannose with acetic anhydride and 1,2-ethanediol. The compound is often referred to by its abbreviation, EEMT.
Synthesis and Characterization:
EEMT can be synthesized using the reaction between D-mannose, acetic anhydride, and 1,2-ethanediol. The reaction takes place at a temperature of 70-80 °C and is catalyzed by a small amount of sulfuric acid. The final product is purified by column chromatography.
The synthesized product can be characterized by various techniques such as infrared spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), and mass spectrometry (MS).
Analytical Methods:
Various analytical methods are used to detect and quantify EEMT in different samples. These methods include:
- High-performance liquid chromatography (HPLC)
- Gas chromatography-mass spectrometry (GC-MS)
- Fourier-transform infrared spectroscopy (FTIR)
- Ultraviolet-visible spectroscopy (UV-Vis)
Biological Properties:
EEMT has been found to have various biological activities such as:
- Anti-tumor activity
- Anti-inflammatory activity
- Anti-viral activity
- Anti-bacterial activity
- Anti-fungal activity
Toxicity and Safety in Scientific Experiments:
Studies have shown that EEMT is relatively safe and non-toxic when used within recommended doses. However, like any other synthetic compound, the safety of EEMT depends on its dosage, duration of exposure, and route of administration. Further studies are needed to establish the exact safety profile of EEMT in different populations.
Applications in Scientific Experiments:
EEMT has various applications in scientific experiments such as:
- As a reagent in carbohydrate chemistry
- As a starting material for the synthesis of other compounds
- As a ligand in metal complex chemistry
- As a chiral auxiliary in asymmetric synthesis
Current State of Research:
EEMT is an active area of research, and various studies are ongoing to explore its potential in different applications. Some of the recent studies include:
- The synthesis of new derivatives of EEMT with enhanced biological activities
- The use of EEMT in the synthesis of chiral molecules
- The investigation of the mechanism of action of EEMT in anti-tumor and anti-inflammatory activities
Potential Implications in Various Fields of Research and Industry:
EEMT has potential implications in various fields of research and industry such as:
- Pharmaceutical industry: EEMT can be used as a starting material for the synthesis of new drugs.
- Chemical industry: EEMT can be used as a reagent in carbohydrate chemistry and metal complex chemistry.
- Agriculture: EEMT can be used as a plant-growth regulator.
Limitations and Future Directions:
Despite the potential of EEMT in different applications, there are some limitations to its use. These include:
- Availability: EEMT is not commercially available in large quantities, and its synthesis is complex and expensive.
- Safety: Further studies are needed to establish the exact safety profile of EEMT in different populations.
Future research directions for EEMT include:
- The investigation of the pharmacological properties of EEMT derivatives.
- The optimization of the synthesis and purification of EEMT.
- The development of new analytical methods for the detection and quantification of EEMT.
In conclusion, EEMT is a versatile compound with potential implications in various fields of research and industry. Further studies are needed to explore its full potential and establish its safety profile.
CAS Number | 28140-37-6 |
Product Name | 1,2-O-(1-Ethoxyethylidene)-beta-D-mannopyranose triacetate |
IUPAC Name | (6,7-diacetyloxy-2-ethoxy-2-methyl-5,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-b]pyran-5-yl)methyl acetate |
Molecular Formula | C16H24O10 |
Molecular Weight | 376.36 g/mol |
InChI | InChI=1S/C16H24O10/c1-6-21-16(5)25-14-13(23-10(4)19)12(22-9(3)18)11(7-20-8(2)17)24-15(14)26-16/h11-15H,6-7H2,1-5H3 |
InChI Key | ULBLUAFHNLHIND-UHFFFAOYSA-N |
SMILES | CCOC1(OC2C(C(C(OC2O1)COC(=O)C)OC(=O)C)OC(=O)C)C |
Canonical SMILES | CCOC1(OC2C(C(C(OC2O1)COC(=O)C)OC(=O)C)OC(=O)C)C |
CAS No: 28140-37-6 MDL No: MFCD01863564 Chemical Formula: C16H24O10 Molecular Weight: 376.36 |
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