Ibogaine hydrochloride

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Identification

Molecular formula
C20H27ClN2O
CAS Number
103740-73-6
IUPAC Name
10-methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium;chloride
Molecular Weight
375.91g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2000g/cm3
Synonyms
1, 2, 3, 4, 5, 6-Hexahydro-10-methoxy-azepino(4, 5-b)indole hydrochloride
Interesting facts

Exploring the Unique World of 10-Methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium; Chloride

This intriguing compound, known as 10-methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium; chloride, holds a fascinating space in the realm of chemical science due to its complex structure and potential applications.

1. Structural Marvel

The compound features a unique bicyclic indole framework combined with a hexahydroazepine ring. This intricate molecular configuration contributes to its distinct properties. Key features include:

  • Indole moiety: A core feature in many biologically active compounds.
  • Hexahydroazepine: Imparts stability and offers a site for further chemical reaction.
  • Methoxy group: Enhances solubility and may affect pharmacological activity.

2. Potential Biological Significance

Compounds that feature the indole structure are often linked to a variety of biological activities. Here are a few noteworthy points:

  • Indoles are frequently found in nature, forming the backbone of many natural products, including neurotransmitters like serotonin.
  • This particular compound’s structure suggests it could participate in interesting interactions with biological targets.
  • Research into related compounds has indicated potential use in fields such as medicinal chemistry and drug discovery.

3. The Role of Chloride

The presence of the chloride ion not only helps in stabilizing the molecule but can also influence its reactivity profile. Chloride ions are known to:

  • Act as a counterion that can facilitate solubility in various solvents.
  • Participate in nucleophilic substitution reactions, potentially leading to novel derivatives.

4. Applications in Research

This compound is of interest mainly in synthetic organic chemistry and pharmacology. Ongoing studies may explore:

  • Its potential as a scaffold for drug design.
  • Interactions with various biological systems, paving the way for future therapeutic developments.
  • Applications in material science due to its unique electronic and structural properties.

In conclusion, 10-methoxy-1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium; chloride offers a wealth of opportunities for further investigation. As scientists continue to explore its properties and potential applications, this compound exemplifies the endless possibilities offered by the chemical universe.

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