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Tabernanthalog

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Identification
Molecular formula
C14H21ClN2
CAS number
1938329-03-9
IUPAC name
3-(1,3-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride
State
State

Tabernanthalog chloride is generally found in a solid state at room temperature.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
232.00
Boiling point (Kelvin)
505.15
General information
Molecular weight
288.80g/mol
Molar mass
288.8000g/mol
Density
1.2203g/cm3
Appearence

Tabernanthalog chloride appears as a crystalline solid at room temperature. It typically forms colorless to pale yellow crystals.

Comment on solubility

Solubility of 3-(1,3-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride

The solubility of 3-(1,3-dimethylpyrrolidin-1-ium-2-yl)-1H-indole;chloride exhibits distinctive characteristics due to its ionic nature. As a quaternary ammonium salt, it is primarily soluble in polar solvents. Here are some key points about its solubility:

  • Water Solubility: This compound is highly soluble in water, facilitating its use in various aqueous applications.
  • Polar Organic Solvents: It shows significant solubility in polar organic solvents like methanol and ethanol.
  • Non-Polar Solvents: Conversely, it presents very low solubility in non-polar solvents such as hexane, reflecting the effects of ionic interactions.

In summary, the solubility of this compound is largely dependent on the solvent's polarity. As stated, “like dissolves like,” emphasizing the compound’s strong affinity for polar solvents while displaying minimal solubility in non-polar environments. This solubility profile can greatly influence its behavior in chemical reactions and applications.

Interesting facts

Interesting Facts about 3-(1,3-Dimethylpyrrolidin-1-ium-2-yl)-1H-Indole; Chloride

The compound known as 3-(1,3-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride is a fascinating entity within the realm of organic chemistry. Its complex structure incorporates both indole and pyrrolidine frameworks, making it a subject of interest in various research fields.

Chemical Characteristics and Applications

  • Complex Structure: The combination of indole, a bicyclic compound known for its role in many natural products and pharmaceuticals, with a pyrrolidine ring adds layers of functionality and versatility to its properties.
  • Bioactive Potential: Indole derivatives are often associated with biological activity, making this compound a candidate for potential pharmacological applications. Research has shown that many indole-based compounds exhibit significant biological properties including anticancer, antimicrobial, and anti-inflammatory activities.
  • Quaternary Ammonium Nature: The presence of the pyrrolidinium moiety indicates that this compound has quaternary ammonium characteristics, which can enhance its solubility in polar solvents, making it an interesting subject for studies involving drug formulation.
  • Research Relevance: This compound may provide insights into new therapeutic agents due to its structural similarity to known bioactive molecules. The indole and pyrrolidine moieties are fundamental in designing novel compounds in medicinal chemistry.

Potential for Future Discoveries

As the field of medicinal chemistry continues to expand, compounds like 3-(1,3-dimethylpyrrolidin-1-ium-2-yl)-1H-indole; chloride may unlock pathways for innovative drug discovery. The exploration of such compounds not only advances our understanding of chemical interactions but also promotes the synthesis of new agents with enhanced efficacy and reduced side effects.

In summary, this compound stands as a testament to the intricate world of chemical compounds and their potential to impact various fields, from medicinal applications to material science. The ongoing research into its properties could reveal critical insights into the development of next-generation pharmaceuticals.

Synonyms
3-(1,3-Dimethyl-2-pyrrolidinyl)indole hydrochloride
19137-92-9
INDOLE, 3-(1,3-DIMETHYL-2-PYRROLIDINYL)-, HYDROCHLORIDE