Compounds > 1-(4,5-dimethoxy-2-nitrophenyl)diazoethane
Page last updated: 2024-12-08
1-(4,5-dimethoxy-2-nitrophenyl)diazoethane
Description
The compound you are referring to is **1-(4,5-dimethoxy-2-nitrophenyl)diazoethane**, also known as **DMNPE**. It's a **diazo compound** often used in **organic synthesis** as a versatile building block for various chemical reactions.
Here's why DMNPE is important for research:
**1. Highly reactive electrophile:** DMNPE is a powerful electrophile, meaning it readily reacts with electron-rich molecules. This makes it an excellent reagent for various reactions like **electrophilic aromatic substitution**, **cycloadditions**, and **alkylation reactions**.
**2. Versatile synthetic tool:** Its reactivity allows researchers to introduce a variety of functional groups into organic molecules, including **nitrogen-containing groups**, **aryl groups**, and **alkyl groups**.
**3. Synthesis of complex molecules:** DMNPE plays a crucial role in the synthesis of complex organic molecules, including **natural products**, **pharmaceuticals**, and **agrochemicals**. This versatility makes it a valuable tool for chemists working in various research areas.
**4. Study of reaction mechanisms:** Due to its unique reactivity, DMNPE is used in studies aimed at understanding reaction mechanisms. Researchers can investigate the steps involved in reactions with DMNPE and gain insight into the principles of organic chemistry.
**Examples of DMNPE applications in research:**
* **Synthesis of pharmaceutical intermediates:** DMNPE has been utilized in the synthesis of various pharmaceutical intermediates, such as those involved in the production of anti-inflammatory drugs, anti-cancer agents, and anti-depressants.
* **Development of new catalysts:** Researchers are exploring the use of DMNPE as a precursor for new catalysts used in various chemical processes.
* **Exploration of new synthetic methodologies:** DMNPE is employed in the development of novel synthetic methods for the preparation of various organic molecules.
**It's important to note:** DMNPE is a highly reactive and potentially hazardous compound. Handling and using it requires proper safety precautions and expert knowledge of its reactivity and potential risks.
1-(4,5-dimethoxy-2-nitrophenyl)diazoethane: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
PubMed CID | 196727 |
MeSH ID | M0225861 |
Synonyms (5)
Synonym |
1-(1-diazoethyl)-4,5-dimethoxy-2-nitrobenzene |
116271-29-5 |
1-(4,5-dimethoxy-2-nitrophenyl)diazoethane |
DTXSID80151327 |
154140-56-4 |
Research Excerpts
Dosage Studied
Research
Studies (9)
Timeframe | Studies, This Drug (%) | All Drugs % |
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (22.22) | 18.2507 |
2000's | 3 (33.33) | 29.6817 |
2010's | 4 (44.44) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 12.27
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
Metric | This Compound (vs All) |
---|
Research Demand Index | 12.27 (24.57) | Research Supply Index | 2.40 (2.92) | Research Growth Index | 4.66 (4.65) | Search Engine Demand Index | 0.00 (26.88) | Search Engine Supply Index | 0.00 (0.95) |
| |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 10 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |