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Benzothiophen-3-ylmethyl-(2-chloroethyl)-ethylammonium chloride

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Identification
Molecular formula
C13H17Cl2NS
CAS number
49670-47-9
IUPAC name
benzothiophen-3-ylmethyl-(2-chloroethyl)-ethyl-ammonium;chloride
State
State

At room temperature, Benzothiophen-3-ylmethyl-(2-chloroethyl)-ethylammonium chloride is typically found as a solid, usually in the form of a crystalline powder.

Melting point (Celsius)
180.50
Melting point (Kelvin)
453.65
Boiling point (Celsius)
344.30
Boiling point (Kelvin)
617.45
General information
Molecular weight
356.89g/mol
Molar mass
356.8860g/mol
Density
1.1540g/cm3
Appearence

Benzothiophen-3-ylmethyl-(2-chloroethyl)-ethylammonium chloride typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of Benzothiophen-3-ylmethyl-(2-chloroethyl)-ethyl-ammonium Chloride

The solubility of benzothiophen-3-ylmethyl-(2-chloroethyl)-ethyl-ammonium chloride (C12H14Cl2N+) can be influenced by several factors, primarily due to its ammonium chloride nature. Here are some key points to consider:

  • Water Solubility: This compound is expected to have good solubility in water owing to the presence of the polar quaternary ammonium structure, which facilitates interaction with water molecules.
  • Solvent Interaction: It may exhibit varying solubility in organic solvents. Polar solvents such as methanol and ethanol might dissolve this compound better than non-polar solvents.
  • Temperature Dependence: As with many ionic compounds, the solubility might increase with temperature. Higher temperatures can enhance the interaction with water molecules, leading to greater dissolution.
  • pH Influence: The solubility can be affected by the pH of the solution. At extreme pH levels, the ionic interactions may alter, impacting its solubility.
  • Order of Magnitude: While specific quantitative solubility data can vary, it is often noted that similar quaternary ammonium salts are generally soluble in aqueous solutions.

In conclusion, the solubility of benzothiophen-3-ylmethyl-(2-chloroethyl)-ethyl-ammonium chloride can be characterized by its strong ability to engage with polar solvents while showcasing sensitivity to temperature and pH variations. Understanding these factors is crucial for practical applications in chemical processes and formulations.

Interesting facts

Exploring Benzothiophen-3-ylmethyl-(2-chloroethyl)-ethyl-ammonium Chloride

Benzothiophen-3-ylmethyl-(2-chloroethyl)-ethyl-ammonium chloride is a fascinating organic compound that merges the unique properties of benzothiophene with the functional characteristics of ammonium compounds. Here are some key points to ponder:

  • Structure and Composition: This compound includes a complex structure, notably featuring both aromatic and aliphatic characteristics due to the benzothiophene and ammonium groups. This unique combination can influence its biological activity.
  • Biological Activity: Compounds of this nature often exhibit interesting pharmacological properties. Studies suggest that derivatives of benzothiophene may contribute to cancer research, potentially acting as anti-cancer agents.
  • Applications in Industry: Beyond pharmaceuticals, benzothiophenes are vital in materials science. They can contribute towards the development of organic semiconductors and other functional materials.
  • Research Interest: The presence of the chlorinated ethyl moiety can enhance the reactivity of the compound, making it an exciting subject for ongoing research in medicinal chemistry.

As scientists explore this compound, the following question arises: How can the properties of benzothiophenes be harnessed for future medical advancements? The potential of this compound lays not just in its chemical structure but in its implications for future innovations.


In summary, benzothiophen-3-ylmethyl-(2-chloroethyl)-ethyl-ammonium chloride is not just another compound in the vast world of chemistry; it represents a confluence of biological potential and industrial applicability. Exploring such novel compounds can lead to groundbreaking discoveries in both scientific research and practical applications.

Synonyms
NSC 84019
BENZO(b)THIOPHENE-3-METHYLAMINE, N-(2-CHLOROETHYL)-N-ETHYL-, HYDROCHLORIDE
7349-45-3
N-(2-Chloroethyl)-N-ethylbenzo(b)thiophene-3-methylamine hydrochloride
Benzo(b)thiophene-3-methanamine, N-(2-chloroethyl)-N-ethyl-, hydrochloride
Benzo(b)thiophene-3-methanamine, N-(2-chloroethyl)-N-ethyl-, hydrochloride (9CI)
1-benzothiophen-3-ylmethyl-(2-chloroethyl)-ethylazanium;chloride