Interesting facts
Interesting Facts about N-(4-chlorophenyl)aziridine-1-carboxamide
N-(4-chlorophenyl)aziridine-1-carboxamide is a fascinating organic compound that belongs to the category of aziridines, which are three-membered nitrogen-containing rings. This compound has garnered attention in various fields of research, particularly due to its unique structural properties and potential applications. Here are some noteworthy aspects:
- Structure and Reactivity: The aziridine ring is known for its strain, making it highly reactive. This compound's structure allows for interesting *nucleophilic reactions* and *ring-opening reactions*, which opens pathways for synthesizing diverse organic molecules.
- Pharmaceutical Potential: Compounds like N-(4-chlorophenyl)aziridine-1-carboxamide are studied for their biological activity. Their structural similarities to various bioactive compounds suggest potential therapeutic applications in medicinal chemistry.
- Research Applications: The compound serves as a valuable intermediate in *synthetic organic chemistry*. Its derivatives may be synthesized to explore their properties and functionalities, providing insights into the development of new materials.
- Role of Chlorine: The presence of a 4-chlorophenyl group is significant as chlorine substitution can influence both reactivity and biological activity. Chlorinated compounds are often noted for their enhanced *lipophilicity* and altered chemical behavior.
- Safety Considerations: As with many chemicals, handling N-(4-chlorophenyl)aziridine-1-carboxamide requires precautions. Knowledge of its reactivity and potential hazards is crucial for safe laboratory practices.
In conclusion, N-(4-chlorophenyl)aziridine-1-carboxamide stands out in organic chemistry, offering intriguing possibilities for research and application. Its unique properties encourage further exploration, making it a subject of considerable scholarly interest.
Synonyms
3647-20-9
1-AZIRIDINECARBOXAMIDE, N-(4-CHLOROPHENYL)-
1-Aziridinecarboxamide, N-(p-chlorophenyl)-
1-(1-Aziridinyl)-N-(p-chlorophenyl)formamide
Formamide, 1-(1-aziridinyl)-N-(p-chlorophenyl)-
WLN: T3NTJ AVMR DG
MLS002694001
NSC-76794
NSC 76794
BRN 0146843
AI3-50723
NSC76794
N-(4-Chlorophenyl)-1-aziridinecarboxamide
9J8LAL6DSR
NCIOpen2_000854
CHEMBL1872999
DTXSID90189979
HMS3094K09
AKOS024385690
SMR001559935
Solubility of N-(4-chlorophenyl)aziridine-1-carboxamide
The solubility of N-(4-chlorophenyl)aziridine-1-carboxamide can vary significantly depending on several factors. While specific empirical data may be limited, we can consider the molecular structure and properties to draw some conclusions.
Factors Influencing Solubility
Given its characteristics, one might expect N-(4-chlorophenyl)aziridine-1-carboxamide to be moderately soluble in polar solvents like water and alcohols, while potentially showing lower solubility in non-polar solvents like hexane.
In summary, understanding the solubility of this compound can be essential for applications in pharmaceuticals and material sciences, making it a subject of interest for further study.