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5-Methoxy-N,N-dimethyltryptamine

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Identification
Molecular formula
C13H18N2S
CAS number
1019-45-0
IUPAC name
N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine
State
State

At room temperature, the compound is typically a solid. The fine crystalline or powdered form generally results in an off-white appearance.

Melting point (Celsius)
115.00
Melting point (Kelvin)
388.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
218.36g/mol
Molar mass
218.3310g/mol
Density
1.2400g/cm3
Appearence

The compound typically appears as a white to off-white powder. It may form crystals depending on the conditions used for purification, and its exact shade can vary slightly depending on impurities or the method of synthesis.

Comment on solubility

Solubility of N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine

N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine is a fascinating compound with interesting solubility characteristics. Understanding its solubility is vital for various applications, particularly in pharmaceuticals and materials science. Here are some key points regarding its solubility:

  • Solvent Dependence: The solubility of this compound can greatly vary depending on the solvent used. It is often soluble in:
    • Polar solvents (e.g., water, methanol)
    • Non-polar solvents (e.g., hexane, chloroform)
  • Temperature Influence: As with many organic compounds, solubility is influenced by temperature. Increasing the temperature typically increases solubility due to enhanced molecular motion.
  • Functional Groups: The presence of functional groups such as the methyl and indole moieties can affect intermolecular interactions, leading to changes in solubility in different environments.

It’s important to note that solubility can also be affected by factors such as *pH*, *ionic strength*, and the presence of other solutes in solution. Therefore, conducting experimentation under varying conditions is essential for obtaining precise solubility data. In conclusion, the solubility of N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine showcases the complexity and intricacy prevalent in chemical compounds, embodying the need for thorough investigation in both laboratory and applied settings.

Interesting facts

Interesting Facts About N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine

N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine is a fascinating compound that belongs to the class of indole derivatives, which are notable for their extensive presence in natural products and biological systems. Here are some captivating insights about this compound:

  • Structural Significance: The indole ring structure plays a vital role in medicinal chemistry, often serving as a scaffold for various pharmacologically active compounds.
  • Biological Activity: Compounds containing indole moieties have been found to exhibit a wide range of biological activities, including anti-inflammatory, anti-cancer, and anti-viral properties.
  • Methylsulfanyl Group: The presence of the methylsulfanyl substituent adds unique properties to this compound, potentially affecting its reactivity and interaction with biological targets.
  • Research Applications: This compound is of significant interest in the pharmaceutical industry, where it might be explored for drug development due to its structural analogies with known therapeutic agents.
  • Challenges and Opportunities: While N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine shows promise, challenges in synthesis and understanding its mechanism of action invite ongoing research in the field of organic and medicinal chemistry.

In summary, N-methyl-2-(5-methylsulfanyl-1H-indol-3-yl)ethanamine is not just a simple compound; it encapsulates a world of possibilities in the intersection of organic synthesis and drug discovery. As researchers delve deeper into its properties, we may uncover even more intriguing applications that could benefit science and medicine alike.

Synonyms
BRN 0394069
INDOLE, 3-(2-(METHYLAMINO)ETHYL)-5-METHYLTHIO-
5564-19-2
3-(2-N-Methylaminoethyl)-5-methylthioindole
DTXSID50204172
5-22-12-00065 (Beilstein Handbook Reference)
DTXCID50126663