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2-(5-Bromobenzothiophen-3-yl)ethyl-dimethylammonium chloride

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Identification
Molecular formula
C12H14BrNS
CAS number
232045-01-7
IUPAC name
2-(5-bromobenzothiophen-3-yl)ethyl-dimethyl-ammonium;chloride
State
State

At room temperature, the compound is typically in a solid state.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
232.00
Boiling point (Kelvin)
505.15
General information
Molecular weight
309.72g/mol
Molar mass
309.7220g/mol
Density
1.5000g/cm3
Appearence

The compound typically appears as a white to off-white solid, often in crystalline form. The exact appearance may vary depending on the method of synthesis and degree of purification.

Comment on solubility

Solubility of 2-(5-bromobenzothiophen-3-yl)ethyl-dimethyl-ammonium;chloride

The compound 2-(5-bromobenzothiophen-3-yl)ethyl-dimethyl-ammonium;chloride tends to exhibit interesting solubility characteristics due to its unique structural features. Understanding its solubility can be helpful for practical applications, such as pharmaceuticals and chemical synthesis.

Solubility Characteristics:

  • Solvent Influence: The presence of the dimethyl-ammonium group suggests that this compound may be more soluble in polar solvents, such as water, due to its ionic nature.
  • Halocyte Interaction: The bromine substituent on the benzothiophene ring may affect how this compound interacts with different solvents, potentially increasing solubility in non-polar solvents as well.
  • pH Dependency: As an ammonium salt, solubility can be influenced by pH levels, possibly becoming more soluble in acidic solutions.

In summary, the solubility of 2-(5-bromobenzothiophen-3-yl)ethyl-dimethyl-ammonium;chloride is expected to be variable:

  1. Higher solubility in polar solvents
  2. Moderate solubility in non-polar solvents
  3. pH-dependent solubility, improving in acidic conditions

Understanding these solubility properties is crucial for researchers and practitioners, as they provide insights into how the compound can be effectively utilized in different chemical environments. As always, experimental validation is essential to fully characterize the solubility behavior of this compound.

Interesting facts

Interesting Facts about 2-(5-Bromobenzothiophen-3-yl)ethyl-dimethyl-ammonium Chloride

2-(5-Bromobenzothiophen-3-yl)ethyl-dimethyl-ammonium chloride (often abbreviated as BTEA) is an intriguing compound that has captured the attention of researchers across various fields of study. Here are some fascinating aspects of this compound:

  • Structural Diversity: BTEA showcases a unique structural arrangement that combines a brominated aromatic system with an ammonium salt. This combination contributes to its diverse reactivity and potential applications.
  • Biological Significance: Compounds containing thiophenes have been researched extensively for their biological activities. BTEA may exhibit interesting pharmacological properties due to the presence of the bromobenzothiophene moiety, which can mimic natural biological pathways.
  • Electrochemical Applications: The ammonium group in BTEA makes it a candidate for electrochemical applications, such as in sensor development and energy storage technologies. These applications can benefit from the ionic properties of the compound.
  • Environmental Impact: With the growing concern for organic pollutants, BTEA could potentially be explored for its ability to interact with various environmental contaminants. Understanding such interactions is crucial for developing better remediation techniques.
  • Synthetic Pathways: The synthesis of BTEA may involve multiple steps, including the bromination of benzothiophene and subsequent alkylation reactions. This synthetic approach provides insights into reaction mechanisms and the handling of reactive intermediates.

In summary, 2-(5-Bromobenzothiophen-3-yl)ethyl-dimethyl-ammonium chloride stands out not only due to its chemical structure but also because of its potential implications in various scientific domains. As research continues to unfold, BTEA could lead to exciting advancements in biological chemistry, material science, and environmental applications.

Synonyms
22964-04-1
5-Bromo-N,N-dimethylbenzo(b)thiophene-3-ethylamine hydrochloride
DTXSID30945657
2-(5-Bromo-1-benzothiophen-3-yl)-N,N-dimethylethan-1-amine--hydrogen chloride (1/1)
RefChem:1061353
BENZO(b)THIOPHENE-3-ETHYLAMINE, 5-BROMO-N,N-DIMETHYL-, HYDROCHLORIDE
DTXCID401373969