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N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine

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Identification
Molecular formula
C15H16N4
CAS number
NA
IUPAC name
N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine
State
State
At room temperature, N2- [2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine is in the solid state as a powder with crystalline properties.
Melting point (Celsius)
178.50
Melting point (Kelvin)
451.65
Boiling point (Celsius)
415.20
Boiling point (Kelvin)
688.35
General information
Molecular weight
250.32g/mol
Molar mass
250.3160g/mol
Density
1.2458g/cm3
Appearence

N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine is a crystalline solid that generally appears as a white to off-white powder. It may have slight discolorations depending on impurities but retains its powdered form under standard conditions.

Comment on solubility

Solubility of N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine

The solubility of N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine in various solvents can greatly influence its application in different fields. Here are some notable points regarding its solubility:

  • Polar Solvents: Typically, compounds with amino and pyridine groups, like this one, exhibit higher solubility in polar solvents due to their ability to form **hydrogen bonds**.
  • Non-Polar Solvents: Conversely, its solubility in non-polar solvents is likely to be *limited* because of the lack of compatible intermolecular interactions.
  • pH Dependency: The pH of the solution can significantly affect solubility, especially for compounds with amine groups, as their protonation state can change.
  • Temperature Influence: As is common with many organic compounds, an increase in temperature may enhance solubility by increasing molecular motion.

In summary, N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine showcases a nuanced behavior in terms of solubility, influenced by its specific structural features and the nature of the solvent.

Interesting facts

Interesting Facts about N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine

N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine is a fascinating compound noteworthy for its structural complexity and potential applications. Here are some intriguing facts about this compound:

  • Structural Diversity: This compound features a unique combination of an indole moiety and a pyridine ring, showcasing the intricate interplay of aromatic systems in organic chemistry.
  • Biological Significance: Compounds similar to this one have been studied for their potential roles in medicinal chemistry, particularly in targeting specific biological pathways and diseases.
  • Research Applications: The unique structure may provide a foundation for the development of novel therapeutic agents, particularly in oncology and neurology.
  • Indole Influence: The indole structure is widely recognized in biochemistry as a building block in numerous biologically active compounds, including tryptophan—a precursor to important neurotransmitters.
  • Potential for Innovation: As a subject of ongoing research, this compound represents an opportunity for chemists to explore new chemical reactions and synthesis methods, enhancing our understanding of organic molecular design.

In summary, N2-[2-(1H-indol-3-yl)ethyl]pyridine-2,3-diamine exemplifies the convergence of chemistry and biology, offering significant avenues for research and application in the medicinal field. Its structural attributes not only present a stimulating challenge for synthetic chemists but may also lead to novel discoveries with far-reaching implications.