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Identification
Molecular formula
C18H28ClNO2S
CAS number
.
IUPAC name
3-(1-methoxycarbonyl-3,3-dimethyl-2-benzothiophen-1-yl)propyl-dimethyl-ammonium;chloride
State
State

The state of this specific compound at room temperature is unknown but similar organic compounds with benzothiophene structures are often solid.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
0.00g/mol
Molar mass
0.0000g/mol
Density
0.0000g/cm3
Appearence

The compound's appearance is not explicitly recorded in any major chemical database, and information might not be publicly available. Usually, such compounds may appear as crystalline solids, powders, or other solid forms, but specifics should be verified through experimental observation or detailed compound-specific studies.

Comment on solubility

Solubility of 3-(1-methoxycarbonyl-3,3-dimethyl-2-benzothiophen-1-yl)propyl-dimethyl-ammonium; chloride

The solubility of this compound, known as 3-(1-methoxycarbonyl-3,3-dimethyl-2-benzothiophen-1-yl)propyl-dimethyl-ammonium; chloride, can be influenced by various factors. Notably, it features an ammonium salt, which generally enhances water solubility compared to neutral compounds.

Factors Affecting Solubility

  • Polarity: The presence of the ammonium group contributes to increased polarity, promoting solubility in polar solvents like water.
  • Temperature: Higher temperatures often increase solubility for many compounds, and this substance may behave similarly.
  • pH Levels: As an ammonium salt, the solubility may also be affected by the acidity or basicity of the solution.

It is worth noting that the presence of bulky groups, such as the 3,3-dimethyl-2-benzothiophen moiety, could hinder the compact packing in a crystalline form, potentially leading to increased solubility. It is often the case that “smaller and less sterically hindered” molecules tend to be more soluble.

In summary, while detailed experimental solubility data might be required for precise applications, the expected trends suggest that this compound could exhibit reasonably good solubility in aqueous environments, with variations based on the metrics outlined above.

Interesting facts

Interesting Facts about 3-(1-methoxycarbonyl-3,3-dimethyl-2-benzothiophen-1-yl)propyl-dimethyl-ammonium;chloride

This compound is a fascinating example of a quaternary ammonium salt, which is known for both its stability and unique structural properties. Let's explore some intriguing aspects:

  • Versatile Applications: Compounds like this one often serve as surfactants, biocides, and even in drug formulation, highlighting their importance in both industrial and pharmaceutical contexts.
  • Complex Structure: The presence of a benzothiophene moiety contributes to its interesting electronic properties, making it a potential candidate for use in organic electronics or as a dye.
  • Mechanism of Action: Quaternary ammonium compounds generally exhibit antimicrobial properties, acting by disrupting microbial membranes, which can be particularly relevant in disinfectants and antiseptics.
  • Tunable Properties: The substituents on the ammonium center allow for the modification of hydrophilicity and hydrophobicity, granting synthetic chemists the ability to tailor compounds for specific applications.

As a chemistry student, one might find it interesting that compounds such as this serve as a reminder of the intricate balance between molecular structure and functionality. Learnings from quaternary ammonium salts are crucial in fields ranging from materials science to medicinal chemistry, making this compound an excellent case study in how chemistry intertwines with everyday applications.

In summary, the study of 3-(1-methoxycarbonyl-3,3-dimethyl-2-benzothiophen-1-yl)propyl-dimethyl-ammonium;chloride offers a glimpse into the diverse world of quaternary ammonium compounds and their significance in various scientific domains.

Synonyms
LU 5-046 hydrochloride
26106-21-8
Benzo(c)thiophene-1-carboxylic acid, 1,3-dihydro-3,3-dimethyl-1-(3-(dimethylamino)propyl)-, methyl ester, hydrochloride
RefChem:351421