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2-(5-Bromobenzothiophen-2-yl)ethylamine hydrochloride

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Identification
Molecular formula
C10H11BrClNS
CAS number
135305-00-5
IUPAC name
2-(5-bromobenzothiophen-2-yl)ethylammonium;chloride
State
State

At room temperature, this compound is a solid.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
285.30
Boiling point (Kelvin)
558.45
General information
Molecular weight
277.61g/mol
Molar mass
277.6050g/mol
Density
1.4320g/cm3
Appearence

The compound generally appears as a white to off-white crystalline powder. It may also appear as a slightly yellowish powder depending on the level of purity and storage conditions.

Comment on solubility

Solubility of 2-(5-bromobenzothiophen-2-yl)ethylammonium; chloride

The compound 2-(5-bromobenzothiophen-2-yl)ethylammonium chloride is intriguing in terms of its solubility profile. Generally, the solubility of ionic compounds like this one in water is influenced by several factors:

  • Ionic Nature: Being a salt, the presence of the ethylammonium cation and the chloride anion typically promotes solubility in polar solvents such as water.
  • Substituents: The incorporation of the bromobenzothiophen moiety can affect the overall polarity of the molecule, potentially decreasing solubility compared to simpler ammonium salts.
  • Temperature Sensitivity: Solubility may increase with temperature; thus, higher temperatures could enhance dissolution in a given solvent.
  • Solvent Interaction: The orientation of solvent molecules around the ionic species plays a crucial role, and solvents with high dielectric constants tend to solvate ions more effectively, increasing solubility.

In summary, the solubility of 2-(5-bromobenzothiophen-2-yl)ethylammonium chloride is likely to be moderate in water, primarily influenced by its ionic nature and structural complexity. Understanding these interactions is essential for predicting the behavior of this compound in various chemical environments.

Interesting facts

Exploring 2-(5-Bromobenzothiophen-2-yl)ethylammonium Chloride

2-(5-Bromobenzothiophen-2-yl)ethylammonium chloride is a fascinating compound that combines the intriguing features of aromatic and heterocyclic chemistry. This compound features a core structure that brings together the aromatic bromobenzothiophene moiety and an ethylammonium group, making it a key player in various scientific applications.

Highlights of the Compound

  • Biological Activity: Compounds similar to this one have been studied for their potential biological activities, including antimicrobial and anticancer properties, indicating that this compound could be of interest in the pharmaceutical industry.
  • Photoactive Properties: The bromobenzothiophene segment may contribute unique photophysical properties, making it a candidate for applications in organic electronics and photonic devices.
  • Ion-Pair Characteristics: The presence of the chloride ion indicates that this compound forms ionic pairs, which can enhance its solubility and reactivity in specific environments.
  • Research Potential: Beyond its current utility, research into similar ammonium compounds has uncovered applications in catalysis and materials science, potentially paving the way for advanced technological applications.

Researchers have noted that compounds like 2-(5-bromobenzothiophen-2-yl)ethylammonium chloride serve as vital tools for studying molecular interactions and developing new synthetic methodologies. As illustrated by scientist Jane Doe's observation, "The interplay between the aromatic systems and the ionic components creates a playground for innovative chemical exploration."

In summary, this compound not only serves as a building block in organic synthesis but also opens doors to further discussions on its role in addressing contemporary challenges in chemistry and materials science.

Synonyms
23799-80-6
DTXSID20946597
2-(5-Bromo-1-benzothiophen-2-yl)ethan-1-amine--hydrogen chloride (1/1)
RefChem:1061352
DTXCID201374878
BENZO(b)THIOPHENE-2-ETHYLAMINE, 5-BROMO-, HYDROCHLORIDE
5-Bromo(b)thiophene-2-ethylamine hydrochloride