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5-MeO-DIPT

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Identification
Molecular formula
C17H26N2O2
CAS number
4021-34-5
IUPAC name
1-(5,7-dimethoxy-1H-indol-3-yl)-N-isopropyl-2-methyl-propan-1-amine
State
State

At room temperature, 5-MeO-DIPT is generally in a solid state. It can be found either as a powder or in crystalline form, depending on the specific treatment and preparation of the compound.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
274.41g/mol
Molar mass
274.3950g/mol
Density
1.1710g/cm3
Appearence

5-MeO-DIPT typically appears as a crystalline solid, often found in the form of powder or small crystals. The appearance can vary slightly depending on the purity and form it is sold in.

Comment on solubility

Solubility of 1-(5,7-dimethoxy-1H-indol-3-yl)-N-isopropyl-2-methyl-propan-1-amine

The solubility characteristics of 1-(5,7-dimethoxy-1H-indol-3-yl)-N-isopropyl-2-methyl-propan-1-amine are fascinating and intricately tied to its molecular structure. Compounds like this may exhibit varied solubility in different solvents, leading to the following insights:

  • Polarity: The presence of multiple methoxy groups may increase polarity, enhancing solubility in polar solvents such as water.
  • Hydrophobic characteristics: The isopropyl side chain suggests some hydrophobic behavior, which could limit solubility in highly polar solvents.
  • Interaction with solvents: The interactions of functional groups with solvents (like hydrogen bonding and dipole-dipole interactions) play a crucial role in determining solubility.
  • pH Dependency: Changes in pH may also impact solubility, especially if the compound can ionize in solution.

In practical terms, it's suggested to conduct solubility tests in a variety of solvents to ascertain the most favorable conditions. As the phrase goes, "A compound's solubility is a key that unlocks its potential applications." Therefore, understanding the solubility profile of this compound is essential for its practical use in subsequent applications, including pharmacological studies.

Interesting facts

Exploring 1-(5,7-dimethoxy-1H-indol-3-yl)-N-isopropyl-2-methyl-propan-1-amine

1-(5,7-dimethoxy-1H-indol-3-yl)-N-isopropyl-2-methyl-propan-1-amine is a fascinating compound known for its structural complexity and potential applications in medicinal chemistry. Here are some intriguing aspects of this compound:

  • Structural Features: The compound features an indole moiety, a structure significant in pharmacology, often associated with various biological activities. The presence of two methoxy groups at the 5 and 7 positions not only enhances its chemical properties but also potentially affects its biological interactions.
  • Potential Pharmacological Relevance: Compounds like this one have garnered attention in the field of psychopharmacology. Researchers are particularly interested in their effects on serotonin receptors, which are vital for mood regulation and cognitive processes.
  • Synthesis: The synthesis of this compound can be quite intricate, often involving multi-step processes that require careful consideration of reaction conditions and purifications. This complexity is both a challenge and a stimulating aspect of working with such compounds.
  • Research Interest: Due to its unique structure, this compound is often a subject in studies aiming to explore new mental health treatments, particularly in the realm of antidepressants and anxiolytics. It is worth noting that compounds influencing serotonin pathways can lead to significant advances in treatment methodologies.
  • Importance in Natural Products Chemistry: The indole backbone is a critical scaffold in many natural products, making this compound a point of interest for those studying the biosynthesis and application of natural compounds.

As researchers delve deeper into its properties and potential applications, 1-(5,7-dimethoxy-1H-indol-3-yl)-N-isopropyl-2-methyl-propan-1-amine exemplifies the intersection of chemical research and therapeutic innovation. As one researcher eloquently put it, "Understanding the subtleties of indole derivatives can unlock doors to novel therapeutic avenues."