N-(3,4-dichlorophenyl)aziridine-1-carboxamide
- Molecular formula
- C9H8Cl2N2O
- CAS Number
- 118292-40-3
- IUPAC Name
- N-(3,4-dichlorophenyl)aziridine-1-carboxamide
- Molecular Weight
- 233.09g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5423g/cm3
- Appearance
- can vary slightly with purity and form.
- Synonyms
- N-(3, 4-Dichlorophenyl)-1-aziridinecarboxamide
Identification
Discovering N-(3,4-Dichlorophenyl)aziridine-1-carboxamide
N-(3,4-Dichlorophenyl)aziridine-1-carboxamide is a fascinating compound with diverse applications in both research and industry. It belongs to the family of aziridines, which are three-membered nitrogen-containing heterocycles known for their unique chemical properties.
Key Features of N-(3,4-Dichlorophenyl)aziridine-1-carboxamide:
- Pharmaceutical Potential: This compound has generated interest in the pharmaceutical industry due to its ability to act as a building block for various medicinally relevant compounds.
- Reactivity: With its strained ring structure, aziridines like this one are highly reactive, making them valuable intermediates in organic synthesis, allowing for the creation of complex molecules.
- Chlorine Substituents: The presence of chlorine atoms on the phenyl ring increases the lipophilicity and potentially alters the biological activity of the compound, warranting further investigation into its mechanisms of action.
- Applications in Material Science: Beyond pharmaceuticals, the structural characteristics of this compound allow it to be explored in the development of new materials, such as polymers and coatings.
As researchers continue to explore its properties, N-(3,4-Dichlorophenyl)aziridine-1-carboxamide exemplifies the intricacies of chemical compounds and their multifaceted roles in advancing science and technology. It serves as a prime example of how a single structure can lead to numerous possibilities, showcasing the importance of investigating even the most niche compounds in the vast field of chemistry.