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5-Methoxytryptophol

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Identification
Molecular formula
C12H15NO2
CAS number
10453-86-8
IUPAC name
2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol
State
State

At room temperature, 5-Methoxytryptophol is typically a solid substance, often found as a crystalline powder.

Melting point (Celsius)
105.00
Melting point (Kelvin)
378.15
Boiling point (Celsius)
188.00
Boiling point (Kelvin)
461.15
General information
Molecular weight
205.26g/mol
Molar mass
206.2470g/mol
Density
1.2040g/cm3
Appearence

5-Methoxytryptophol is typically seen as a crystalline solid compound. It may appear in powdered form or as clear prismatic crystals depending on purity and method of preparation.

Comment on solubility

Solubility of 2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol

2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol exhibits interesting solubility characteristics that can vary significantly depending on the solvent used. Here are some key points to consider:

  • Polar Solvents: This compound is likely to be soluble in polar solvents such as water and methanol due to the presence of amino and alcohol functional groups which can engage in hydrogen bonding.
  • Non-Polar Solvents: Conversely, its solubility in non-polar solvents (like hexane or benzene) is expected to be low because the structure contains polar regions that do not favor non-polar environments.
  • pH Sensitivity: The solubility can also be influenced by the pH of the solution. At lower pH levels, the amine group may become protonated, potentially improving solubility in aqueous solutions.

In conclusion, the solubility of 2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol is defined by its chemical structure that promotes dissolution in polar solvents while limiting solubility in non-polar solvents. Understanding these solubility dynamics is crucial for applications in both laboratory and industrial settings.

Interesting facts

Interesting Facts about 2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol

2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol is a fascinating compound with a variety of features worth noting:

  • Complex Structure: This compound contains an indole moiety, which is fundamental in many biologically active compounds. Indoles are known for their roles in neurotransmitter functions and regulation.
  • Biosynthesis: The incorporation of an amino group alongside the wood-like methoxy group suggests a potential pathway for biosynthesis in natural systems. Indole derivatives, often found in plant alkaloids, illustrate the ecological importance of this structure.
  • Pharmacological Potential: Due to its structural components, this compound may exhibit interesting pharmacological properties. Compounds related to indole and amino alcohols are prevalent in medicinal chemistry, often serving as precursors or active agents in pharmaceuticals.
  • Research Interest: Recent studies have explored the neuroprotective and autophagy-enhancing effects of similar compounds, suggesting that this particular compound might contribute valuable insights in drug discovery.
  • Versatility: The presence of both amino and phenolic functionalities within the compound gives it potential for interaction with a variety of biological systems, making it a valuable candidate for further investigation in biochemistry and pharmacology.

In sum, 2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol is not just a chemical entity; it represents a nexus of interdisciplinary research opportunities spanning organic chemistry, pharmacology, and environmental science. As scientists delve deeper into its properties, we may uncover even more applications and implications in health and nature.

Synonyms
beta-Amino-5-methoxy-1H-indole-3-propanol
20913-94-4
BRN 0192163
2-amino-3-(5-methoxy-1H-indol-3-yl)propan-1-ol
1H-INDOLE-3-PROPANOL, beta-AMINO-5-METHOXY-
SCHEMBL4749748
DTXSID10943176
5-22-12-00358 (Beilstein Handbook Reference)