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5-MeO-MIPT

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Identification
Molecular formula
C15H22N2O
CAS number
96096-55-8
IUPAC name
5-methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole
State
State

At room temperature, 5-MeO-MIPT is typically a solid. It usually occurs as a powder or crystalline substance.

Melting point (Celsius)
104.00
Melting point (Kelvin)
377.15
Boiling point (Celsius)
379.50
Boiling point (Kelvin)
652.65
General information
Molecular weight
246.36g/mol
Molar mass
246.3310g/mol
Density
1.1600g/cm3
Appearence

5-MeO-MIPT appears as a white solid when in pure form. The compound is often synthesized as a crystalline powder or in solid crystals.

Comment on solubility

Solubility of 5-methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole

When discussing the solubility of 5-methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole, several key factors must be considered:

  • Polarity: The presence of both hydrophobic and hydrophilic groups in this compound impacts its solubility in various solvents.
  • Solvent Choice: This compound may display different solubility profiles in:
    • Polar solvents: It tends to have lower solubility due to less interaction with the solvent molecules.
    • Non-polar solvents: It is more likely to be soluble here, aligning with its hydrophobic characteristics.
  • Temperature Influence: Generally, increasing temperature can enhance the solubility of organic compounds.
  • pH Effects: The solubility may change under different pH conditions, especially if the compound can ionize.

Overall, the solubility of 5-methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole is complex and context-dependent. As a rule of thumb, "like dissolves like" serves as a foundational principle—meaning that this compound is more soluble in non-polar solvents where it can interact favorably.

Interesting facts

Fascinating Insights into 5-Methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole

5-Methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole is a remarkable chemical compound that has inspired interest across various fields of study, especially in medicinal chemistry and pharmacology. Here are some intriguing aspects of this compound:

  • Indole Backbone: This compound features an indole structure, which is a core component in many biologically active compounds. Indoles are known for their prevalence in natural products and their significant presence in pharmaceuticals.
  • Psychoactive Potential: Compounds like this one are of great interest due to their potential psychoactive properties. The inclusion of a pyrrolidine ring suggests possible interactions with neurotransmitters, which may influence mood and cognition.
  • Research Applications: Scientists are investigating compounds with similar structures for their potential roles in treating neurological disorders, indicating a promising avenue for therapeutic development.
  • Structural Diversity: The unique combination of a methoxy group and pyrrolidine substitution creates a diverse structural profile, highlighting the versatility of indole derivatives in medicinal chemistry.
  • Bioactivity: Initial studies suggest that compounds like 5-methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole could exhibit bioactive properties, paving the way for potential new drugs.

“Understanding the intricate relationships between structure and activity is crucial in drug design.” This quote resonates particularly well with the study of compounds like this, as structural modifications can lead to vastly different pharmacological profiles.

Overall, 5-methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole exemplifies the rich tapestry of organic chemistry, reminding researchers of the importance of exploring the vast potential embedded within complex molecular architectures.

Synonyms
19137-94-1
3-(N-Methylpyrrolidin-2-ylmethyl)-5-methoxyindole
3-MPMMeO-indole
RefChem:92704
5-methoxy-3-(1-methylpyrrolidin-2-yl)-1H-indole
BRN 0749171
5-Methoxy-3-(1-methyl-2-pyrrolidinyl)indole
5-Methoxy-3-(1-methyl-2-pyrrolidinyl)-1H-indole
DTXSID60940751
INDOLE, 5-METHOXY-3-(1-METHYL-2-PYRROLIDINYL)-