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Dimethylbenzothiophenium chloride

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Identification
Molecular formula
C19H24ClNS
CAS number
98627-30-0
IUPAC name
dimethyl-[3-(1-phenyl-3H-2-benzothiophen-1-yl)propyl]ammonium;chloride
State
State

At room temperature, dimethylbenzothiophenium chloride is typically found as a solid. The compound is stable under normal conditions but should be stored in a cool, dry place to maintain its integrity and prevent any reaction with moisture or other environmental factors.

Melting point (Celsius)
116.00
Melting point (Kelvin)
389.00
Boiling point (Celsius)
278.00
Boiling point (Kelvin)
551.00
General information
Molecular weight
333.88g/mol
Molar mass
333.8750g/mol
Density
1.2000g/cm3
Appearence

Dimethylbenzothiophenium chloride typically appears as a crystalline solid that can be white or off-white in color. It may also appear as a powder depending on its preparation and storage conditions. Its crystalline nature is indicative of its ionic structure derived from the quarternary ammonium salt.

Comment on solubility

Solubility of Dimethyl-[3-(1-phenyl-3H-2-benzothiophen-1-yl)propyl]ammonium Chloride

The solubility of dimethyl-[3-(1-phenyl-3H-2-benzothiophen-1-yl)propyl]ammonium chloride can be influenced by various factors due to its complex molecular structure. Understanding its solubility is crucial for both practical applications and theoretical chemistry considerations.

Factors Affecting Solubility

  • Polarity: The presence of the ammonium group generally enhances solubility in polar solvents such as water.
  • Hydrophobic Portions: The benzothiophene moiety contributes to hydrophobicity, which can limit solubility in more polar environments.
  • Temperature: Solubility may increase with temperature, although the specific behavior depends on the interactions between solute and solvent.

General Observations

In general, salts like chlorides tend to be soluble in water; however, the additional large organic groups in this compound may create significant hydrophobic characteristics. Therefore, you might find that:

  • It is soluble in organic solvents (like ethanol or acetone) due to its large hydrophobic regions.
  • It has limited solubility in water without specific solubilizing agents.

As a result, while we can expect a degree of solubility consistent with ammonium salts, precise measurements would depend on the solvent system and environmental conditions. Exploring these interactions can lead to a better understanding of the compound's potential applications in pharmaceutical or materials science.

Interesting facts

Interesting Facts about Dimethyl-[3-(1-phenyl-3H-2-benzothiophen-1-yl)propyl]ammonium Chloride

Dimethyl-[3-(1-phenyl-3H-2-benzothiophen-1-yl)propyl]ammonium chloride is a fascinating compound that demonstrates the intriguing intersection of organic chemistry and pharmacology. Here are some key facts that make this compound noteworthy:

  • Quaternary Ammonium Compound: This compound is categorized as a quaternary ammonium salt, which means it features a positively charged nitrogen atom bonded to four organic groups. This structure often imparts interesting properties and biological activities.
  • Potential Biological Activity: Compounds like dimethyl-[3-(1-phenyl-3H-2-benzothiophen-1-yl)propyl]ammonium chloride may exhibit notable pharmacological effects, including potential antitumor and antimicrobial activities, which are subjects of ongoing research.
  • Structural Complexity: The unique presence of the benzothiophene moiety not only contributes to the compound's distinct chemical behavior but also makes it a key point of interest in medicinal chemistry. The sulfur atom in the benzothiophene enhances the compound's electronic properties.
  • Applications in Research: Researchers are continually exploring the applications of this compound in drug design and development, particularly in the synthesis of new pharmaceuticals that could lead to more effective treatments for various diseases.
  • Synthetic Routes: The synthesis of such complex compounds often involves intricate organic reactions, providing a valuable opportunity for students and chemists to hone their skills in synthetic methodology.

In conclusion, dimethyl-[3-(1-phenyl-3H-2-benzothiophen-1-yl)propyl]ammonium chloride is not just a chemical entity; it is a gateway to potential insights in both synthetic chemistry and biological applications. As researchers delve deeper into its properties and effects, we may unlock new therapeutic opportunities that could benefit society.

Synonyms
LU 4-064 hydrochloride
26106-00-3
RefChem:1088572
1,3-Dihydro-N,N-dimethyl-1-phenylbenzo(c)thiophene-1-propylamine hydrochloride
Benzo(c)thiophene-1-propylamine, 1,3-dihydro-N,N-dimethyl-1-phenyl-, hydrochloride