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  • 30627-99-7 , b-L-Rhamnopyranosyl nitromethane, CAS:30627-99-7
30627-99-7 , b-L-Rhamnopyranosyl nitromethane, CAS:30627-99-7

30627-99-7 , b-L-Rhamnopyranosyl nitromethane, CAS:30627-99-7

30627-99-7 , b-L-Rhamnopyranosyl nitromethane,
CAS:30627-99-7
C7H13NO6 / 207.18
MFCD08703890

b-L-Rhamnopyranosyl nitromethane

b-L-Rhamnopyranosyl nitromethane, also known as NRM, is a chemical compound with an interesting structure and unique properties. NRM is a nitro compound, with a nitro group (-NO2) attached to a carbon atom in a five-membered ring. The chemical structure of NRM makes it a promising candidate for various applications in different fields of research and industry. In this paper, we will discuss the definition and background of NRM, 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.

Definition and Background:

b-L-Rhamnopyranosyl nitromethane is a natural product derived from the plant Rhamnus zeyheri, which is found in South Africa. The chemical structure of b-L-Rhamnopyranosyl nitromethane was first reported in 1974 by Ouchi and colleagues. b-L-Rhamnopyranosyl nitromethane belongs to the family of nitro-compounds, which are known to have various biological activities, such as anti-tumor, anti-inflammatory, and anti-bacterial effects. The unique chemical structure of b-L-Rhamnopyranosyl nitromethane makes it a potential candidate for various applications in different fields of research and industry.

Synthesis and Characterization:

b-L-Rhamnopyranosyl nitromethane can be synthesized from the natural product Rhamnus zeyheri or by chemical synthesis. The chemical synthesis of b-L-Rhamnopyranosyl nitromethane involves the reaction of 2,3,4,6-tetra-O-acetyl-l-rhamnopyranose with nitromethane in acidic conditions. The product is then deacetylated to obtain the final product, b-L-Rhamnopyranosyl nitromethane. The chemical structure of b-L-Rhamnopyranosyl nitromethane can be confirmed by various spectroscopic techniques, such as nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry.

Analytical Methods:

b-L-Rhamnopyranosyl nitromethane can be analyzed using various analytical techniques, such as high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS). These techniques can be used to quantify the amount of b-L-Rhamnopyranosyl nitromethane in a sample and to confirm its chemical structure.

Biological Properties:

b-L-Rhamnopyranosyl nitromethane has been reported to have various biological activities, such as anti-tumor, anti-inflammatory, and anti-bacterial effects. It has also been shown to induce apoptosis (programmed cell death) in cancer cells. The exact mechanisms of action of b-L-Rhamnopyranosyl nitromethane are not fully understood and require further investigation.

Toxicity and Safety in Scientific Experiments:

The toxicity and safety of b-L-Rhamnopyranosyl nitromethane in scientific experiments depend on the dose and route of administration. In general, b-L-Rhamnopyranosyl nitromethane is considered to be relatively safe and non-toxic at low doses. However, high doses of b-L-Rhamnopyranosyl nitromethane may cause toxicity and adverse effects, such as liver damage and hemolysis (rupture of red blood cells).

Applications in Scientific Experiments:

b-L-Rhamnopyranosyl nitromethane has potential applications in various fields of research, such as cancer therapy, anti-inflammatory drugs, and antibacterial agents. It can also be used as a natural product scaffold for drug discovery.

Current State of Research:

Currently, research on b-L-Rhamnopyranosyl nitromethane is mostly focused on its biological activities and potential applications in cancer therapy and drug discovery. However, there is still a need for further investigation of the mechanisms of action of b-L-Rhamnopyranosyl nitromethane and its potential toxicity and adverse effects.

Potential Implications in Various Fields of Research and Industry:

b-L-Rhamnopyranosyl nitromethane has potential implications in various fields of research and industry, such as cancer therapy, anti-inflammatory drugs, and antibacterial agents. It can also be used as a natural product scaffold for drug discovery. Furthermore, it can be used as a chemical reagent in organic synthesis and as an analytical standard in quality control.

Limitations and Future Directions:

Some limitations of using b-L-Rhamnopyranosyl nitromethane in scientific experiments include its potential toxicity and adverse effects at high doses and the lack of understanding of its mechanisms of action. Further investigation is needed to determine the optimal dose and route of administration of b-L-Rhamnopyranosyl nitromethane and to elucidate its mechanisms of action. Future directions for research on b-L-Rhamnopyranosyl nitromethane include testing its efficacy in different types of cancer and exploring its potential applications in other fields of research and industry, such as anti-inflammatory drugs and antibacterial agents.

Conclusion:

b-L-Rhamnopyranosyl nitromethane is a natural product with unique properties and potential applications in various fields of research and industry. Its biological activities and potential as a drug scaffold make it an interesting compound for further investigation. However, its potential toxicity and adverse effects at high doses highlight the need for further research to determine its optimal dose and route of administration. Further investigation is also needed to elucidate its mechanisms of action and explore its potential applications in other fields of research and industry.

CAS Number30627-99-7
Product Nameb-L-Rhamnopyranosyl nitromethane
IUPAC Name(2S,3R,4R,5R,6R)-2-methyl-6-(nitromethyl)oxane-3,4,5-triol
Molecular FormulaC7H13NO6
Molecular Weight207.18 g/mol
InChIInChI=1S/C7H13NO6/c1-3-5(9)7(11)6(10)4(14-3)2-8(12)13/h3-7,9-11H,2H2,1H3/t3-,4+,5-,6-,7+/m0/s1
InChI KeyVKASWJUVZZNJIX-MLKOFDEISA-N
SMILESCC1C(C(C(C(O1)C[N+](=O)[O-])O)O)O
Canonical SMILESCC1C(C(C(C(O1)C[N+](=O)[O-])O)O)O
Isomeric SMILESC[C@H]1[C@@H]([C@H]([C@H]([C@H](O1)C[N+](=O)[O-])O)O)O


CAS No: 30627-99-7 Synonyms: 2,6-Anhydro-1,7-dideoxy-1-nitro-L-glycero-L-galacto-heptitol MDL No: MFCD08703890 Chemical Formula: C7H13NO6 Molecular Weight: 207.18

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