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Harmane

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Identification
Molecular formula
C12H10N2
CAS number
486-84-0
IUPAC name
1-methyl-2H-pyrido[3,4-b]indole
State
State

At room temperature, harmane is a solid.

Melting point (Celsius)
228.00
Melting point (Kelvin)
501.15
Boiling point (Celsius)
395.00
Boiling point (Kelvin)
668.15
General information
Molecular weight
182.22g/mol
Molar mass
182.2240g/mol
Density
1.1898g/cm3
Appearence

Harmane appears as a white to light yellow crystalline powder. It is known for its characteristic fluorescence under UV light, often appearing blue or blue-violet.

Comment on solubility

Solubility of 1-methyl-2H-pyrido[3,4-b]indole

The solubility of 1-methyl-2H-pyrido[3,4-b]indole can be quite intriguing, as its behavior in various solvents can tell us much about its chemical nature.

In general, this compound exhibits the following solubility characteristics:

  • Solvent Polarity: It is anticipated that 1-methyl-2H-pyrido[3,4-b]indole will be more soluble in non-polar solvents due to its aromatic structure, which suggests a strong tendency to interact with similar non-polar environments.
  • Temperature Dependency: Solubility may increase with temperature, a common characteristic seen in organic compounds, as higher temperatures allow for greater molecular interactions and dissolution.
  • pH Influence: The solubility might be affected by the pH of the solution if functional groups capable of protonation or deprotonation are present; however, the structure of this compound suggests it might be relatively stable across a range of pH levels.

In summary, the solubility of 1-methyl-2H-pyrido[3,4-b]indole is expected to be influenced by both the solvent type and environmental conditions. As a rule of thumb, "like dissolves like," making it essential to choose appropriate solvents for effective dissolution.

Interesting facts

Interesting Facts About 1-methyl-2H-pyrido[3,4-b]indole

1-methyl-2H-pyrido[3,4-b]indole is a fascinating compound that belongs to the family of heterocyclic compounds, specifically indoles. This compound is known for its unique structure and intriguing properties, which make it a subject of interest in various fields of research.

Key Highlights:

  • Structural Characteristics: The molecule features a pyridoindole framework resulting from the fusion of a pyridine ring and an indole structure, which contributes to its rich chemical behavior.
  • Biological Relevance: Research has shown that analogs of 1-methyl-2H-pyrido[3,4-b]indole exhibit potential biological activity, making them interesting candidates for pharmacological studies.
  • Applications: This compound may be explored in the fields of medicinal chemistry, particularly in the development of new drugs targeting various diseases.
  • Research Significance: Studies into this compound contribute to our understanding of polycyclic aromatic compounds, which can be crucial for environmental chemistry and toxicity assessments.

As a chemistry student or scientist, exploring the mechanisms of such compounds can unveil novel insights into their interactions and functionalities. The intricate structure of 1-methyl-2H-pyrido[3,4-b]indole not only enhances its reactivity but also raises questions about its potential synthetic routes and modifications that can lead to new derivatives with enhanced properties.

In summary, 1-methyl-2H-pyrido[3,4-b]indole is more than just a chemical formula; it represents a blend of chemistry, biology, and pharmacology that continues to inspire research and innovation in the field.