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5-Hydroxytryptophol propanoate

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Identification
Molecular formula
C13H16N2O2
CAS number
2276-23-3
IUPAC name
[3-(2-aminoethyl)-1H-indol-5-yl] propanoate
State
State

Solid

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
221.29g/mol
Molar mass
221.2650g/mol
Density
1.2200g/cm3
Appearence

A white to off-white crystalline solid.

Comment on solubility

Solubility of [3-(2-aminoethyl)-1H-indol-5-yl] propanoate

The solubility of [3-(2-aminoethyl)-1H-indol-5-yl] propanoate can be influenced by various factors, including pH, temperature, and the presence of other solvents. Understanding its solubility behavior is crucial for its application in pharmaceuticals and biochemistry. Here are some key considerations:

  • Polarity: As an organic compound, its solubility in water may be limited due to its relatively non-polar characteristics.
  • Temperature Dependence: Generally, solubility may increase with temperature. Thus, studying the temperature profile is important for practical applications.
  • pH Sensitivity: The presence of amino groups can make the compound behave differently across various pH levels. For instance:
    • At low pH, the amino group may become protonated, potentially increasing solubility in aqueous solutions.
    • At neutral to high pH, the compound may exist in a less soluble form.
  • Solvent Compatibility: It may exhibit better solubility in organic solvents like ethanol or methanol compared to water due to its structural nature.

In summary, the solubility of [3-(2-aminoethyl)-1H-indol-5-yl] propanoate is a multifaceted topic that requires attention to polarity, temperature, pH, and solvent interactions. Understanding these parameters can lead to more effective usage and application in various fields.

Interesting facts

Interesting Facts about [3-(2-aminoethyl)-1H-indol-5-yl] propanoate

[3-(2-aminoethyl)-1H-indol-5-yl] propanoate, often referred to within certain scientific circles, is a compound that stands out due to its unique structural properties and potential applications. Here are some intriguing points worth noting:

  • Structural Diversity: This compound features an indole moiety, which is a bicyclic structure consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. Indole derivatives are particularly noteworthy for their presence in various biological systems.
  • Biological Relevance: The presence of the aminoethyl group suggests potential interactions with biological targets. Many indole derivatives are known to exhibit significant pharmacological activities, including anti-inflammatory and anti-cancer properties.
  • Research Interest: Compounds like [3-(2-aminoethyl)-1H-indol-5-yl] propanoate are often studied in the context of drug discovery and development. Researchers are increasingly focusing on the synthesis and modification of indole-based compounds to enhance their efficacy and specificity.
  • Versatile Synthesis: The synthesis of [3-(2-aminoethyl)-1H-indol-5-yl] propanoate typically involves various organic reactions, making it a compound of interest in synthetic organic chemistry. Its synthesis may serve as a model for developing related compounds.

In the words of chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." The exploration of compounds like [3-(2-aminoethyl)-1H-indol-5-yl] propanoate certainly contributes to the tapestry of knowledge in the field of chemistry. As scientists continue to unravel the complexities of such compounds, their potential applications could lead to numerous advancements in medicinal chemistry and beyond.