3-Chlorophenylaziridine-1-carboxylate

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Identification

Molecular formula
C10H10ClNO
CAS Number
13228-39-2
IUPAC Name
aziridin-1-yl-(3-chlorophenyl)methanone
Molecular Weight
183.64g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3000g/cm3
Synonyms
20286-18-4
Interesting facts

Interesting Facts about Aziridin-1-yl-(3-chlorophenyl)methanone

Aziridin-1-yl-(3-chlorophenyl)methanone is a fascinating compound that has garnered attention in the field of medicinal chemistry. Its unique structure and functional groups contribute to various properties that make it significant in pharmaceutical applications.

Key Features of Aziridin-1-yl-(3-chlorophenyl)methanone

  • Structural Significance: The presence of an aziridine ring adds strain and reactivity, which can be advantageous in organic synthesis and drug development.
  • Medicinal Potential: Compounds featuring chlorophenyl groups often exhibit engaging biological activities, making them potential candidates for therapeutic agents.
  • Reactivity: The electrophilic character of the carbonyl group in the methanone allows for various reactions, including nucleophilic additions and other functionalization processes.
  • Versatile Applications: Research has indicated applications in fields such as agriculture for pest control and in the synthesis of more complex molecules.

As a part of ongoing studies, scientists are exploring the interactions of this compound with biological systems. The use of aziridin-1-yl derivatives in anticancer research is particularly notable, as they may modify cellular processes in targeted ways. “The intersection of aziridine chemistry and pharmacology opens exciting avenues for innovative drug discovery,” states a prominent researcher in the field.

In conclusion, aziridin-1-yl-(3-chlorophenyl)methanone exemplifies the synergy between structure and function in chemical compounds, inviting further exploration into its potential applications and biological impact.

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