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1-Methyl-1,2,3,4-tetrahydro-β-carboline chloride

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Identification
Molecular formula
C13H18ClN2
CAS number
93456-69-8
IUPAC name
3,6-dimethyl-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-6-ium;chloride
State
State
Solid at room temperature.
Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.15
General information
Molecular weight
235.75g/mol
Molar mass
337.8750g/mol
Density
1.2200g/cm3
Appearence

The compound typically appears as a crystalline solid or powder. It is generally white or off-white in color.

Comment on solubility

Solubility of 3,6-dimethyl-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-6-ium;chloride

The solubility of 3,6-dimethyl-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-6-ium;chloride can be influenced by several factors:

  • Polarity: Being a quaternary ammonium salt, the chloride form typically exhibits higher solubility in polar solvents, particularly water, due to the ionic interactions.
  • Temperature: Increased temperature generally enhances solubility as it provides energy that helps break intermolecular forces.
  • pH Levels: The solubility can vary with changes in pH, as this can impact the ionic state of the compound.
  • Presence of Other Solutes: The 'common ion effect' may play a role, whereby the presence of certain ions in solution can decrease solubility.

In summary, one might say, "the solubility can be abundant in appropriate environments but may exhibit limitations under certain conditions." The specifics of solubility should always be experimentally determined for accurate applications.

Interesting facts

Interesting Facts about 3,6-dimethyl-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-6-ium Chloride

This fascinating compound, known as a member of the azepine family, is a complex structure that showcases the interplay between aromatic and aliphatic regions within organic chemistry. It features an indole scaffold that is fundamental to many biologically active molecules, making it a point of interest for research and development.

Key Features:

  • Cyclic Structure: The azepine portion contributes to the unique cyclic structure, often resulting in distinct reactivity patterns and properties.
  • Heteroatom Influence: The presence of nitrogen in the ring enhances its potential for biological activity, often improving solubility and interaction with biological targets.
  • Methyl Groups: The dimethyl substitutions at the 3 and 6 positions provide steric hindrance, which can influence the compound's reactivity and stability.

Applications:

Due to its complex structure, this compound may exhibit a variety of interesting properties and applications:

  • Potential use in pharmaceutical development as new drugs targeting specific biological pathways.
  • Valuable in materials science for synthesizing novel polymers or conducting materials.
  • Basic research in organic synthesis for developing new methodologies in producing complex molecules.

“The chemistry of heterocycles is a cornerstone in organic synthesis and medicinal chemistry. Understanding how these complex structures behave is critical for innovation.”

In conclusion, 3,6-dimethyl-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-6-ium chloride stands as a compelling example of how intricate organic compounds can open doors to numerous scientific fields, making it an exciting compound for chemists to study and utilize.

Synonyms
1,2,3,4,5,6-Hexahydro-3,6-dimethyl-azepino(4,5-b)indole hydrochloride
15918-75-9
AZEPINO(4,5-b)INDOLE, 1,2,3,4,5,6-HEXAHYDRO-3,6-DIMETHYL-, MONOHYDROCHLORIDE