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N-(3,4-dichlorophenyl)aziridine-1-carboxamide

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Identification
Molecular formula
C9H8Cl2N2O
CAS number
118292-40-3
IUPAC name
N-(3,4-dichlorophenyl)aziridine-1-carboxamide
State
State

At room temperature, N-(3,4-dichlorophenyl)aziridine-1-carboxamide is a solid with high stability. In ambient conditions, it remains a solid, cautiously stable under recommended storage conditions.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
215.00
Boiling point (Kelvin)
488.15
General information
Molecular weight
233.09g/mol
Molar mass
233.0900g/mol
Density
1.5423g/cm3
Appearence

The compound N-(3,4-dichlorophenyl)aziridine-1-carboxamide typically appears as a white to off-white solid. The material may be crystalline in nature and its appearance can vary slightly with purity and form.

Comment on solubility

Solubility of N-(3,4-dichlorophenyl)aziridine-1-carboxamide

N-(3,4-dichlorophenyl)aziridine-1-carboxamide is a compound whose solubility can be influenced by several factors. Understanding the solubility profile of this molecule is key to its potential applications in various fields. Here are some important points to consider:

  • Polarity: The presence of both a polar carboxamide group and a hydrophobic dichlorophenyl moiety means solubility may vary significantly in different solvents.
  • Solvent Interaction: This compound is likely to be more soluble in polar solvents such as water or DMSO compared to non-polar solvents due to the polar nature of the carboxamide group.
  • Temperature Effects: Solubility often increases with temperature; therefore, conducting experiments at elevated temperatures could reveal higher solubility values.
  • pH Sensitivity: The solubility might be influenced by pH, particularly due to the ionizable nature of the carboxamide functional group if it interacts with acids or bases.

In conclusion, the solubility of N-(3,4-dichlorophenyl)aziridine-1-carboxamide can vary widely based on its interactions with different solvents and environmental conditions. As stated in scientific literature, “As the polarity increases, solubility in polar solvents tends to follow,” making it crucial to consider these factors for effective applications.

Interesting facts

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.

Synonyms
N-(3,4-Dichlorophenyl)-1-aziridinecarboxamide
15460-48-7
N-(3,4-dichlorophenyl)aziridine-1-carboxamide
3,4-Dichlorophenyl-N-carbamoylaziridine
1-AZIRIDINECARBOXAMIDE, N-(3,4-DICHLOROPHENYL)-
BRN 0166483
AI3-51773
ZY5MK8F9DH
SCHEMBL27979643
DTXSID90165672
Dichlorophenyl-N-carbamoylaziridine, 3,4-