Skip to main content

5-Methoxy-N,N-dimethyltryptamine

ADVERTISEMENT
Identification
Molecular formula
C15H20N2O
CAS number
3023-26-7
IUPAC name
5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole
State
State

At room temperature, 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole is typically found in a solid state.

Melting point (Celsius)
65.00
Melting point (Kelvin)
338.15
Boiling point (Celsius)
312.50
Boiling point (Kelvin)
585.70
General information
Molecular weight
246.34g/mol
Molar mass
246.3370g/mol
Density
1.1900g/cm3
Appearence

5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole typically appears as a crystalline solid that can vary in color from white to off-white. The compound is often used in research and can have slight variations in appearance depending on its purity and the method of production.

Comment on solubility

Solubility of 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole

The solubility of 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole can be quite variable depending on multiple factors such as the solvent, temperature, and pH of the solution. This compound, known for its complex indole structure, presents unique solubility characteristics:

  • Polar Solvents: Generally, compounds that bear polar functional groups tend to dissolve better in polar solvents such as water or ethanol.
  • Non-Polar Solvents: Conversely, the hydrophobic regions in the molecule might promote better solubility in non-polar solvents like chloroform or dichloromethane.
  • Temperature Dependence: As temperature increases, the solubility often increases for solid solutes. Thus, heating the solvent may enhance the solubility of this compound.
  • pH Effects: The ionization state of the molecule can significantly influence its solubility. Adjusting the pH of the solution may help in optimizing the solubility.

It is important to assess the solubility in various conditions to fully understand how well 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole can be utilized in synthetic and analytical applications. As a general rule of thumb, "like dissolves like,” which highlights the need to match the polarity of the solvent to that of the compound for optimal solubility.

In conclusion, the solubility of this compound can be both challenging and fascinating, requiring careful consideration of the solvent environment.

Interesting facts

Interesting Facts about 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole

5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole is a fascinating compound with a growing interest in both the scientific community and the pharmaceutical industry. Here are some notable aspects:

  • Structure and Composition: This compound features an indole ring system, which is a core structure in many natural and synthetic products. The presence of a methoxy group and a pyrrolidine moiety adds a unique character to its chemical behavior and potential interactions.
  • Biological Activity: Compounds containing indole structures have been extensively studied for their various biological properties. Due to the presence of the pyrrolidine group, this compound may exhibit interesting neuroactive effects, potentially influencing neurotransmitter systems.
  • Applications: In drug development, structures like 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole can serve as templates for designing new medications. These types of indoles are often explored for their roles in treating conditions such as depression and anxiety.
  • Research Interest: The exploration of compounds that include both indole and pyrrolidine units has led to breakthroughs in understanding complex biological pathways. Such compounds can be pivotal in the study of receptor binding and signal transduction.
  • Integration in Natural Products: Indole derivatives are frequently found in numerous alkaloids and are essential in many medicinal plants, highlighting their significance in traditional medicine and their potential for new drug discovery.

In summary, the study of 5-methoxy-3-(2-pyrrolidin-1-ylethyl)-1H-indole reflects the intricate world of organic chemistry and its implications in health sciences. Quoting Albert Einstein, "The greatest scientists are artists as well." This compound exemplifies the beauty of molecular design and natural inspiration in science.

Synonyms
3949-14-2
CT 4436
5-Methoxy-3-(2-pyrrolidinoethyl)indole
5-Methoxy-3-[2-(1-pyrrolidinyl)ethyl]-1H-indole
Methoxy-5-pyrrolidino-2'-ethyl-3-indole
INDOLE, 5-METHOXY-3-(2-(1-PYRROLIDINYL)ETHYL)-
5-MEO-PYR-T
CHEMBL608537
5-methoxy-3-(2-(pyrrolidin-1-yl)ethyl)-1H-indole
BRN 0479607
NCIOpen2_005795
SCHEMBL24723815
DTXSID50192626
KAASYKNZNPWPQG-UHFFFAOYSA-N
BDBM50474416
HY-W728110
PD212912
DB-382737
Q4639628