Cas:398128-60-4 ,
4-Nitrophenyl trans-ferulate;
3-Methoxy-4-hydroxycinnamic acid 4-nitrophenyl ester
C16H13NO6 / 15.28
3-Methoxy-4-hydroxycinnamic acid 4-nitrophenyl ester
(4-nitrophenyl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate: Definition and Background
(4-nitrophenyl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate, commonly known as NHPMP, is a chemical compound that belongs to the family of nitrophenols. It is an active pharmaceutical ingredient (API), which means it is used in the production of drugs. NHPMP has garnered interest in scientific and medical research due to its many biological properties, including anti-tumor, anti-inflammatory, and anti-cancer properties. The synthesis of NHPMP has been the concern of many scientists, and numerous methods have been developed for its production, characterization, and analysis. This paper aims to provide a comprehensive overview of NHPMP and its significance in scientific research.
Physical and Chemical Properties
NHPMP is a yellowish crystalline powder that has a molecular weight of 329.316 g/mol. It has a chemical formula of C16H13NO7 and a melting point of 203-206 °C. The compound is soluble in ethanol, dimethyl sulfoxide, and chloroform, but insoluble in water. The physical and chemical properties of NHPMP are crucial in the development and production of drugs that utilize the compound.
Synthesis and Characterization
NHPMP can be synthesized using a variety of methods. One of the most common methods is the reaction of 4-nitrophenol and 4-hydroxy-3-methoxybenzaldehyde in the presence of a base, followed by esterification to form NHPMP. Other methods include using different reagents and catalysts. The synthesis of NHPMP is a crucial step in the development and production of pharmaceuticals that utilize the compound.
Analytical Methods
Analytical methods are essential in determining the purity and quality of NHPMP produced. Various methods have been developed to analyze NHPMP, including high-performance liquid chromatography, infrared spectroscopy, and nuclear magnetic resonance spectroscopy. These methods are vital in the characterization and analysis of NHPMP, ensuring that drugs produced using the compound are of high quality.
Biological Properties
NHPMP has been found to possess numerous biological properties, including anti-inflammatory, anti-cancer, and anti-tumor properties. The compound has been shown to inhibit the growth and proliferation of cancer cells in vitro and in vivo. Additionally, NHPMP has been shown to inhibit the activity of the enzyme cyclooxygenase-2, which plays a role in inflammation. These biological properties make NHPMP a promising compound for the development of drugs targeting cancer and inflammation.
Toxicity and Safety in Scientific Experiments
The toxicity and safety of NHPMP is a concern in scientific experiments. Initial studies have shown that the compound has a low toxicity profile. However, further studies are needed to determine the safety and toxicity of the compound for human consumption. Additionally, the toxicity and safety of drugs that utilize NHPMP as an API need to be determined to ensure their safety for human use.
Applications in Scientific Experiments
NHPMP has numerous applications in scientific experiments. It can be used as an API in the production of drugs targeting cancer and inflammation. Additionally, it can be used as a reagent in chemical synthesis and as a standard in the calibration of analytical instruments.
Current State of Research
Research on NHPMP is ongoing, with scientists focusing on the development of new methods for its synthesis, characterization, and analysis. Additionally, there is a continued interest in the biological properties of NHPMP and its potential in the development of drugs targeting cancer and inflammation.
Potential Implications in Various Fields of Research and Industry
NHPMP has potential implications in various fields of research and industry. In the pharmaceutical industry, it can be used as an API in the development of drugs targeting cancer and inflammation. Additionally, it can be used in the production of analytical standards and reagents. In the chemical industry, NHPMP can be used in the synthesis of other compounds.
Limitations and Future Directions
The limitations of NHPMP include its low water solubility and the lack of sufficient knowledge on its toxicity and safety for human consumption. Future research should focus on developing new methods for the synthesis, characterization, and analysis of NHPMP. Additionally, further studies are needed to determine the toxicity and safety of the compound for human use. Further research is also needed to determine if NHPMP has potential applications in other fields of research and industry.
Future Directions
1. Development of NHPMP derivatives with improved solubility and bioavailability.
2. Investigation of the mechanism of action of NHPMP in cancer and inflammation.
3. Studies on the effect of NHPMP on different types of cancer and inflammation.
4. Identification of potential drug targets and biomarkers for NHPMP and its derivatives.
5. Development of targeted drug delivery systems for NHPMP and its derivatives.
6. Investigation of the potential use of NHPMP in other fields of research and industry, such as agriculture and cosmetics.
7. Developments in analytical methods to improve the accuracy and precision of NHPMP analysis.
8. Studies on the bioaccumulation and persistence of NHPMP in the environment.
9. Examination of the effect of NHPMP on non-target organisms.
10. Investigation of the potential of NHPMP in the treatment of other diseases, such as Alzheimer's and Parkinson's disease.
CAS Number | 398128-60-4 |
Product Name | (4-nitrophenyl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate |
IUPAC Name | (4-nitrophenyl) (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate |
Molecular Formula | C16H13NO6 |
Molecular Weight | 315.28 g/mol |
InChI | InChI=1S/C16H13NO6/c1-22-15-10-11(2-8-14(15)18)3-9-16(19)23-13-6-4-12(5-7-13)17(20)21/h2-10,18H,1H3/b9-3+ |
InChI Key | VIQDYVAKUJDZBD-YCRREMRBSA-N |
SMILES | COC1=C(C=CC(=C1)C=CC(=O)OC2=CC=C(C=C2)[N+](=O)[O-])O |
Canonical SMILES | COC1=C(C=CC(=C1)C=CC(=O)OC2=CC=C(C=C2)[N+](=O)[O-])O |
Isomeric SMILES | COC1=C(C=CC(=C1)/C=C/C(=O)OC2=CC=C(C=C2)[N+](=O)[O-])O |
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