Skip to main content

Betahistine hydrochloride

ADVERTISEMENT
Identification
Molecular formula
C12H18ClNOS
CAS number
5638-76-6
IUPAC name
1-(benzothiophen-3-yl)-2-pyrrolidin-1-ium-1-yl-ethanol;chloride
State
State

At room temperature, Betahistine hydrochloride is typically a solid.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
239.75g/mol
Molar mass
239.7530g/mol
Density
1.4825g/cm3
Appearence

Betahistine hydrochloride typically appears as a white to off-white crystalline powder.

Comment on solubility

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

The solubility of 1-(benzothiophen-3-yl)-2-pyrrolidin-1-ium-1-yl-ethanol;chloride can be significantly influenced by its unique chemical structure. This compound, comprising both a cationic and an anionic component, usually exhibits moderate to high solubility in polar solvents. Here are some key points regarding its solubility:

  • Solvent Compatibility: The compound is likely to be soluble in water due to its ionic nature stemming from the chloride anion, which promotes hydration.
  • Organic Solvents: Additionally, it may demonstrate solubility in polar organic solvents such as ethanol and methanol, which can stabilize its ionic components.
  • Temperature Effects: Like many ionic compounds, solubility may increase with temperature; thus, higher temperatures could lead to enhanced solubility.

In conclusion, the solubility characteristics of 1-(benzothiophen-3-yl)-2-pyrrolidin-1-ium-1-yl-ethanol;chloride are predominantly determined by its ionic interactions and the nature of the solvent. Understanding these factors is crucial for applications in both pharmaceuticals and materials science.

Interesting facts

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

This intriguing compound, known as 1-(benzothiophen-3-yl)-2-pyrrolidin-1-ium-1-yl-ethanol; chloride, showcases the fascinating interplay between organic chemistry and medicinal applications. Here are some noteworthy insights:

  • Structural Complexity: The compound features a unique combination of a benzothiophene moiety fused with a pyrrolidine ring, creating an intricate structure that potentially contributes to its chemical behavior and biological activity.
  • Pharmaceutical Potential: Compounds with similar structures have been explored for their therapeutic applications, particularly in neuropharmacology. They might exhibit properties that make them candidates for developing new drugs targeting neurological disorders.
  • Chloride Feature: The presence of the chloride ion is significant as it can influence the solubility and reactivity of the compound, essential for its interaction with biological systems.
  • Unique Reactivity: The pyrrolidine ring adds a layer of reactivity to the molecule, allowing for various substitutions and modifications which are critical in synthetic organic chemistry.
  • Research Interest: The study of such compounds can improve our understanding of their mechanism of action, leading to insights that could pave the way for innovative therapeutic strategies.

In the exploration of this compound, researchers often emphasize its potential in drug design, indicating that further investigations might reveal beneficial properties that could contribute to advancements in medicinal chemistry.

Synonyms
alpha-(Pyrrolidinomethyl)benzo(b)thiophene-3-methanol hydrochloride
7349-53-3
BENZO(b)THIOPHENE-3-METHANOL, alpha-(PYRROLIDINOMETHYL)-, HYDROCHLORIDE