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INDAPARSTAT

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Identification
Molecular formula
C15H12N3
CAS number
25104-18-1
IUPAC name
1-(1H-indol-3-yl)-N-(2-pyridyl)methanimine
State
State
Solid at room temperature. Typically powder or crystalline form.
Melting point (Celsius)
90.00
Melting point (Kelvin)
363.20
Boiling point (Celsius)
357.50
Boiling point (Kelvin)
630.60
General information
Molecular weight
233.28g/mol
Molar mass
233.2830g/mol
Density
1.2200g/cm3
Appearence

The compound is typically a solid powder. Its color can vary from white to off-white, sometimes appearing as a pale crystalline solid, depending on its purity and physical form.

Comment on solubility

Solubility of 1-(1H-indol-3-yl)-N-(2-pyridyl)methanimine

The solubility of 1-(1H-indol-3-yl)-N-(2-pyridyl)methanimine can be influenced by several factors, primarily its chemical structure and the surrounding environmental conditions. This compound possesses both hydrophilic and hydrophobic characteristics due to its indole and pyridine rings, which can affect its interaction with solvents.

Key Points to Consider:

  • Solvent Type: Generally, organic compounds with aromatic rings tend to exhibit limited solubility in water but can dissolve well in polar organic solvents such as methanol, ethanol, and dimethyl sulfoxide (DMSO).
  • Temperature: Increased temperature often enhances solubility by providing the energy needed for solute-solvent interactions. This phenomenon can be particularly relevant for this compound.
  • pH Level: The solubility can also change with variations in pH, particularly if functional groups are protonatable.

In summary, while 1-(1H-indol-3-yl)-N-(2-pyridyl)methanimine may show limited aqueous solubility, its behavior in organic solvents is generally more favorable. This dual nature can be utilized in various applications, making solubility a critical factor to consider when working with this compound.

Interesting facts

Interesting Facts about 1-(1H-indol-3-yl)-N-(2-pyridyl)methanimine

This fascinating compound presents a confluence of two important aromatic structures: the indole and pyridine rings. As a member of the class of compounds known as methanimines, it exhibits a unique combination of properties that may have significant implications in various fields of research.

Chemical Context

  • Indole Structure: The indole moiety is known for its presence in many biologically active compounds, including neurotransmitters such as serotonin.
  • Pyridine Influence: The incorporation of a pyridine ring contributes to enhanced stability and specific reactivity, making it a valuable component in pharmaceuticals.
  • Versatility: Methanimines are known for their potential in organic synthesis, paving the way for creating complex molecules.

Biological Relevance

This compound's structure suggests potential biological activity. The combination of the indole and pyridine rings may lead researchers to investigate its roles as:

  • Antioxidants: Exploring the compound's capacity to neutralize free radicals.
  • Pharmacological Agents: Considering its potential in the development of new drugs targeting various diseases.
  • Biological Markers: Investigating its role in biochemical pathways related to cancer or neurological functions.

Research Insights

The compound opens the door for interdisciplinary research opportunities. Some intriguing points for further study include:

  • Synthetic Pathways: The exploration of innovative methods to synthesize this compound can advance organic chemistry.
  • Structure-Activity Relationship: Understanding how variations in its structure may influence biological activity could enhance drug design efforts.
  • Material Science: Potential applications in creating new materials due to its chemical properties.

As researchers continue to delve into the fascinating world of heterocyclic compounds like 1-(1H-indol-3-yl)-N-(2-pyridyl)methanimine, there is much to discover. Its rich structural basis not only promises potential applicability in medicinal chemistry but also fascinates the scientific community with its myriad possibilities!