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Benzothiophene ethanol chloride

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Identification
Molecular formula
C15H21ClNOS
CAS number
902841-42-1
IUPAC name
1-(benzothiophen-3-yl)-2-piperidin-1-ium-1-yl-ethanol;chloride
State
State

At room temperature, Benzothiophene ethanol chloride exists as a solid, due to its stable crystalline structure.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
297.00
Boiling point (Kelvin)
570.15
General information
Molecular weight
288.82g/mol
Molar mass
288.8150g/mol
Density
1.2780g/cm3
Appearence

The compound is typically observed as a solid, crystalline powder, often appearing white or off-white in color. It may have a slight aromatic odor, characteristic of many organic compounds containing benzothiophene groups.

Comment on solubility

Solubility of 1-(benzothiophen-3-yl)-2-piperidin-1-ium-1-yl-ethanol;chloride

The solubility of 1-(benzothiophen-3-yl)-2-piperidin-1-ium-1-yl-ethanol;chloride is influenced by several factors due to its unique structure and ionic nature.

Factors Affecting Solubility

  • Ionic Character: As a salt (chloride), its solubility is generally enhanced in polar solvents, particularly water.
  • Functional Groups: The presence of the benzothiophen moiety may introduce hydrophobic characteristics, affecting overall solubility.
  • Temperature: Like many chemical compounds, solubility tends to increase with temperature; thus, higher temperatures may lead to a greater dissolution rate.

In summary, while 1-(benzothiophen-3-yl)-2-piperidin-1-ium-1-yl-ethanol;chloride demonstrates moderate water solubility due to its ionic nature, the specific solubility profile will depend on the balance of hydrophilic and hydrophobic interactions. It is essential to consider the solvent choices and environmental conditions to fully understand its solubility behavior.

Interesting facts

Interesting Facts about 1-(Benzothiophen-3-yl)-2-piperidin-1-ium-1-yl-ethanol; Chloride

This intriguing compound, often referred to as a synthetic derivative, holds a significant place in the realm of medicinal chemistry. Its unique structure features a junction between a benzothiophene moiety and a piperidine ring, which contributes to its diverse biological activities.

Chemical Structure and Properties

The compound's complex framework allows for interesting interactions in biological systems. Key points to note include:

  • Benzothiophene component: This aromatic structure contributes to the compound's potential as a pharmacological agent.
  • Piperidine ring: Known for its ability to interact with various receptors, this part may enhance the biological activity of the molecule.
  • Chloride ion: The presence of the chloride counter ion can affect solubility and stability, which are critical for drug efficacy.

Biological Significance

The compound has drawn interest due to its potential therapeutic applications. Some noted effects include:

  • Neuroactive properties: It may exhibit activity that influences neurotransmission, presenting possibilities for treating neurological disorders.
  • Anti-inflammatory effects: Research indicates that similar compounds can reduce inflammatory responses within biological systems.
  • Psychoactive potential: Some derivatives in this class have been studied for their psychoactive effects, raising interest in their use for certain mental health conditions.

Conclusion

Considering 1-(benzothiophen-3-yl)-2-piperidin-1-ium-1-yl-ethanol;chloride, its unique structural attributes and potential applications make it a compound of great interest in the fields of pharmaceutical research and medicinal chemistry. As scientists continue to explore its properties, it may pave the way toward novel therapeutic solutions.

Synonyms
alpha-(Piperidinomethyl)benzo(b)thiophene-3-methanol hydrochloride
7384-97-6
BENZO(b)THIOPHENE-3-METHANOL, alpha-(PIPERIDINOMETHYL)-, HYDROCHLORIDE