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4-arsoroso-N,N-bis(2-chloroethyl)aniline

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Identification
Molecular formula
C10H13AsCl2NO
CAS number
330-60-5
IUPAC name
4-arsoroso-N,N-bis(2-chloroethyl)aniline
State
State

At room temperature, this compound is a solid that may gradually decompose when exposed to atmospheric conditions.

Melting point (Celsius)
111.00
Melting point (Kelvin)
384.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
288.60g/mol
Molar mass
288.6040g/mol
Density
1.4500g/cm3
Appearence

4-Arsoroso-N,N-bis(2-chloroethyl)aniline appears as a crystalline solid that can range in color from off-white to pale yellow. It is sensitive to light and air, which can cause it to darken over time.

Comment on solubility

Solubility of 4-arsoroso-N,N-bis(2-chloroethyl)aniline

The solubility of 4-arsoroso-N,N-bis(2-chloroethyl)aniline is an interesting phenomenon influenced by various factors. As a chemical compound that contains both aromatic and aliphatic components, its solubility can be assessed in different solvents under varying conditions.

Key Factors Affecting Solubility:

  • Polarity: The presence of polar groups in the structure can enhance solubility in polar solvents, while nonpolar regions may favor solubility in nonpolar solvents.
  • Temperature: Solubility typically increases with temperature, making it essential to consider the thermal conditions when assessing the solubility of this compound.
  • pH Level: The solubility can also be affected by the pH of the solution, which may impact the ionization of functional groups within the compound.

For practical applications, it's worth noting that 4-arsoroso-N,N-bis(2-chloroethyl)aniline may exhibit limited solubility in water. Therefore, it is often advisable to explore organic solvents such as dimethyl sulfoxide (DMSO) or acetone for more effective solubilization.

In summary, while the exact solubility of this compound may vary based on experimental conditions, understanding the interplay of these factors can guide effective use in chemical processes and applications.

Interesting facts

Interesting Facts about 4-arsoroso-N,N-bis(2-chloroethyl)aniline

4-arsoroso-N,N-bis(2-chloroethyl)aniline is a fascinating compound that draws interest from the fields of chemistry, pharmacology, and environmental science. Below are some intriguing points about this compound:

  • Organometallic Connection: This compound contains a significant amount of arsenic, which can be both beneficial and toxic, depending on its form and concentration.
  • Potential Applications: Due to its unique chemical structure, 4-arsoroso-N,N-bis(2-chloroethyl)aniline is often studied for its potential use in medicinal chemistry, particularly in the development of new pharmaceuticals targeting specific diseases.
  • Environmental Concerns: Compounds containing arsenic are known to pose serious environmental risks. Understanding their behavior in ecosystems is crucial to mitigating their impact.
  • Synthesis: The production of this compound involves sophisticated organic synthesis techniques, which are pivotal for aspiring chemists to master.
  • Safety Precautions: Working with arsenic-based compounds necessitates robust safety protocols due to their toxicity; chemists must adhere strictly to laboratory safety guidelines.

In summary, the synthesis and research surrounding 4-arsoroso-N,N-bis(2-chloroethyl)aniline provide vital insights into the interplay of organic chemistry and toxicology. As highlighted by one research study, "The intricate design of arsenic-containing compounds opens new avenues for therapeutic discovery while demanding unwavering attention to safety and environmental stewardship."


Through ongoing inquiry, the dual nature of compounds like this continues to shape our understanding of chemistry's role in health and safety.

Synonyms
BRN 2849283
ANILINE, p-ARSENOSO-N,N-BIS(2-CHLOROETHYL)-
4164-07-2
p-Arsenoso-N,N-bis(2-chloroethyl)aniline
DTXSID00194453
DTXCID10116944