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Indolizino[3,2-b][1]benzazepin-16-ium chloride

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Identification
Molecular formula
C13H16ClN2
CAS number
1256580-46-7
IUPAC name
1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium;chloride
State
State

At room temperature, this compound is typically found in a solid state. It typically appears as a crystalline powder, reflecting incident light with a glossy sheen.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
251.74g/mol
Molar mass
251.7380g/mol
Density
1.1990g/cm3
Appearence

The compound typically appears as a crystalline solid, often forming colorless to pale yellow crystals. Its appearance may vary slightly depending on the specific method of synthesis and purity, but it is generally a clear crystalline substance in solid form.

Comment on solubility

Solubility of 1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium;chloride

The solubility of 1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium;chloride in various solvents is a topic of significant interest due to its potential applications. The solubility of this compound can be influenced by several factors:

  • Polarity of the solvent: Generally, this compound is expected to be more soluble in polar solvents such as water and alcohols compared to non-polar solvents.
  • Ionization: As a chloride salt, the ionization in aqueous solutions leads to increased solubility. The presence of chloride ions can enhance solvation.
  • Temperature: Solubility often increases with temperature. Warm solutions may dissolve this compound more effectively.

Furthermore, it is important to note that solubility may vary with pH levels, as acidic or basic environments can affect the ionization state of the compound. In conclusion, while the solubility of 1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium;chloride could exhibit favorable characteristics in water and other polar solvents, practical experimentation would be essential to identify precise solubility limits and conditions.

Interesting facts

Interesting Facts about 1,2,3,4,5,6-Hexahydroazepino[4,5-b]indol-6-ium; Chloride

The compound known as 1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium; chloride is a fascinating member of the fused ring systems, specifically involving nitrogen heterocycles. Its structure showcases the complexity that can arise in organic chemistry, particularly in medicinal chemistry, where it holds potential significance.

Key Features:

  • Cyclic Structure: This compound features a unique cyclic structure that contributes to its distinct properties and potential applications.
  • Biological Activity: Compounds with similar indole structures are known to exhibit a variety of biological activities, making them valuable in drug discovery.
  • Chloride Salt Form: Being in the chloride salt form can enhance the solubility and bioavailability of the compound, which is a crucial factor in pharmacological studies.
  • Research Application: This compound may serve as a scaffold for the development of new pharmaceuticals, especially in treating neurological disorders.

As a species in the indole family, its reactivity can also be influenced by the incorporation of nitrogen within the fused ring system. Researchers are continuously exploring its potential as a therapeutic candidate, and ongoing studies aim to unlock further secrets held within its molecular architecture.

Quote from a Chemist: "Exploring the vast landscape of nitrogen heterocycles like this compound gives us insight into novel therapeutic avenues that could lead to breakthroughs in medicine."

In summary, 1,2,3,4,5,6-hexahydroazepino[4,5-b]indol-6-ium; chloride exemplifies the rich interplay between structure and function in organic compounds, embodying the essence of scientific inquiry in the field of chemistry.

Synonyms
1,2,3,4,5,6-Hexahydro-azepino(4,5-b)indole hydrochloride
15923-41-8
AZEPINO(4,5-b)INDOLE, 1,2,3,4,5,6-HEXAHYDRO-, MONOHYDROCHLORIDE