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5-Methylthio-DMT

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Identification
Molecular formula
C13H18N2S
CAS number
92292-84-7
IUPAC name
1-(5-methylsulfanyl-1H-indol-3-yl)propan-2-amine
State
State

This compound is typically found in a solid state at room temperature, usually as a crystalline powder.

Melting point (Celsius)
143.00
Melting point (Kelvin)
416.15
Boiling point (Celsius)
293.15
Boiling point (Kelvin)
566.30
General information
Molecular weight
234.36g/mol
Molar mass
234.3550g/mol
Density
1.2200g/cm3
Appearence

5-Methylthio-DMT typically appears as a white crystalline powder. It is a derivative of the tryptamine alkaloid and can also be found in the form of crystalline solids.

Comment on solubility

Solubility of 1-(5-methylsulfanyl-1H-indol-3-yl)propan-2-amine

The solubility of 1-(5-methylsulfanyl-1H-indol-3-yl)propan-2-amine can be influenced by various factors, which makes its behavior in solvents a subject of interest.

  • Polarity: Due to the presence of amine and sulfur functional groups in its structure, the compound is likely to exhibit polar characteristics, affecting its ability to dissolve in polar solvents like water.
  • Solvent Type: It may have varying solubility in different solvents; for instance, it might be more soluble in organic solvents such as ethanol or DMSO compared to water.
  • Temperature Influence: As with many organic compounds, solubility can increase with temperature, enhancing interactions with solvent molecules.

In many cases with similar compounds, the degree of solubility can be crucial for applications, especially in pharmaceuticals, where solubility affects bioavailability and therapeutic effectiveness. Therefore, understanding the solubility profile of 1-(5-methylsulfanyl-1H-indol-3-yl)propan-2-amine is essential for predicting its behavior in various environments.


Interesting facts

Interesting Facts about 1-(5-methylsulfanyl-1H-indol-3-yl)propan-2-amine

1-(5-methylsulfanyl-1H-indol-3-yl)propan-2-amine is a compound that captivates scientists due to its intriguing structural features and potential applications. Here are some interesting points about this unique compound:

  • Indole Moiety: The indole structure, known for its aromaticity, plays a significant role in various biological activities. Indoles are known to be involved in the formation of important natural products and pharmaceuticals.
  • Amino Functionality: The presence of the amine group contributes to its basic nature and ability to form hydrogen bonds, which can enhance its reactivity and interactions with other compounds.
  • Sulfur Atom: The methylsulfanyl group not only modifies its chemical properties, but it may also contribute to the compound's biological effects. Compounds containing sulfur are often associated with medicinal properties.
  • Potential Pharmacological Activity: Due to its unique structure, this compound may exhibit a variety of effects, including neuroprotective and antidepressant-like activities, drawing interest from researchers exploring therapeutic avenues.
  • Novelty in Synthesis: The synthesis of compounds like 1-(5-methylsulfanyl-1H-indol-3-yl)propan-2-amine often involves innovative methodologies, making it a subject of study in synthetic organic chemistry.

As a research target, this compound represents an exciting intersection of chemistry and pharmacology, where understanding its properties could lead to advancements in drug discovery and development. As with many compounds, ongoing research will shed light on its full potential and applications in various fields.

Synonyms
5102-06-7
3-(2-Aminopropyl)-5-methylthioindole
BRN 0396209
3-(2-Amino-1-propyl)-5-(methylthio)indole
INDOLE, 3-(2-AMINO-1-PROPYL)-5-METHYLTHIO-
DTXSID30965294
1-[5-(methylsulfanyl)-1H-indol-3-yl]propan-2-amine