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Eupatorin

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Identification
Molecular formula
C24H25N4O10S
CAS number
38444-84-5
IUPAC name
[2-(benzothiophen-3-yl)-2-hydroxy-ethyl]-dimethyl-ammonium;2,4,6-trinitrophenolate
State
State

This compound is typically found as a solid at room temperature.

Melting point (Celsius)
101.00
Melting point (Kelvin)
374.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
258.03g/mol
Molar mass
258.0300g/mol
Density
1.6150g/cm3
Appearence

It appears as a yellow to greenish-yellow crystalline solid.

Comment on solubility

Solubility of [2-(benzothiophen-3-yl)-2-hydroxy-ethyl]-dimethyl-ammonium;2,4,6-trinitrophenolate

The solubility of the compound [2-(benzothiophen-3-yl)-2-hydroxy-ethyl]-dimethyl-ammonium; 2,4,6-trinitrophenolate is influenced by its unique molecular structure and the interactions between its components. Understanding its solubility characteristics can provide insights into its chemical behavior and application potential. Here are some key points to consider:

  • Water Solubility: Compounds with ammonium groups often exhibit increased solubility in water due to their ability to form hydrogen bonds with water molecules.
  • Influence of Functional Groups: The presence of the -OH group may enhance solubility, as hydroxyl groups are typically polar.
  • Effect of Benzothiophen Ring: The aromatic ring system can introduce hydrophobic characteristics, potentially decreasing solubility in polar solvents.
  • Challenging Solubility Profile: The combination of the hydrophilic ammonium group and the hydrophobic benzothiophen moiety creates a complex solubility profile, likely leading to variable solubility in different solvents.

In summary, while the ammonium and -OH groups suggest a degree of solubility, the overall solubility of this compound will depend significantly on the solvent used. For practical applications, it is crucial to conduct empirical tests to establish specific solubility values and behaviors.

Interesting facts

Interesting Facts about [2-(benzothiophen-3-yl)-2-hydroxy-ethyl]-dimethyl-ammonium;2,4,6-trinitrophenolate

This intriguing compound showcases the fascinating intersection of organic chemistry and pharmacology. Known for its unique molecular structure, it has garnered attention for its potential applications in various fields. Here are some noteworthy points:

  • Dual Role: This compound functions as both a cationic agent due to its ammonium group and as a complex anionic component linked to the 2,4,6-trinitrophenolate moiety, demonstrating how different functional groups can interact within a single molecule.
  • Potential Therapeutics: Compounds of this nature, particularly with the benzothiophene framework, are often studied for their biological activities including anti-inflammatory and antitumor properties, making them of interest to medicinal chemists worldwide.
  • Intriguing Synthesis: The synthesis of such compounds typically involves advanced organic synthesis techniques, which can include multi-step reactions. This not only emphasizes the creativity required in organic chemistry but also the precision needed in handling sensitive reagents.
  • Environmental Applications: Due to the presence of nitro groups, such compounds can also be investigated for their reactivity and potential as intermediates in the synthesis of other chemical entities, as well as their role in environmental chemistry.
  • Ubiquitous Research: Ongoing studies focus on understanding the various reactivity patterns and the potential for derivatives of this compound to enhance its effectiveness or selectivity in biological systems.

In summary, [2-(benzothiophen-3-yl)-2-hydroxy-ethyl]-dimethyl-ammonium;2,4,6-trinitrophenolate is a representation of the complexity of chemical compounds that hold significant promise in both research and applications. As scientists delve deeper into its properties and potential, we may witness breakthroughs that could redefine its role in various industries.

Synonyms
alpha-(Dimethylaminomethyl)benzo(b)thiophene-3-methanol picrate
7565-81-3
BENZO(b)THIOPHENE-3-METHANOL, alpha-(DIMETHYLAMINOMETHYL)-, PICRATE