N-(4-nitrophenyl)aziridine-1-carboxamide
ADVERTISEMENT
- Molecular formula
- C9H9N3O3
- CAS Number
- 4808-76-4
- IUPAC Name
- N-(4-nitrophenyl)aziridine-1-carboxamide
- Molecular Weight
- 207.18g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3812g/cm3
- Synonyms
- 3647-22-1
Identification
Interesting facts
Interesting Facts about N-(4-nitrophenyl)aziridine-1-carboxamide
N-(4-nitrophenyl)aziridine-1-carboxamide is a fascinating compound owing to its unique structure and potential applications in various fields of chemistry and pharmaceuticals. Here are some noteworthy highlights:
- Structural Uniqueness: This compound features an aziridine ring, which is a three-membered cyclic amine. The incorporation of the 4-nitrophenyl group adds a powerful electron-withdrawing effect, making the compound highly reactive.
- Potential Uses: Due to its reactivity, N-(4-nitrophenyl)aziridine-1-carboxamide is of interest in medicinal chemistry as a potential precursor in the synthesis of biologically active molecules.
- Biological Activity: Compounds containing aziridine structures are often explored for their antiviral and anticancer properties, providing a pathway toward new therapeutic agents.
- Elasticity Challenge: The strained aziridine ring makes this compound susceptible to ring-opening reactions, a feature that chemists can use to their advantage in synthetic pathways.
- A Synthetic Curiosity: The methods of synthesizing this compound often involve complex multistep reactions, making it a compelling study subject for students and researchers seeking to understand advanced organic synthesis techniques.
As you delve deeper into the structure and reactivity of N-(4-nitrophenyl)aziridine-1-carboxamide, you’ll uncover the intricate relationships between its unique molecular features and its biological implications. The journey of studying this compound is not only intellectually stimulating but also opens up avenues for groundbreaking discoveries in the world of chemistry.