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AB-PINACA

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Identification
Molecular formula
C22H26N2O
CAS number
1445752-09-9
IUPAC name
3-(1-butylpyrrolidin-2-yl)-1H-indole
State
State

The compound is typically found in a solid state at room temperature, most commonly as a powder.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.20
Boiling point (Celsius)
785.10
Boiling point (Kelvin)
1 058.20
General information
Molecular weight
331.47g/mol
Molar mass
331.4720g/mol
Density
1.0460g/cm3
Appearence

AB-PINACA appears as a powdered substance that can vary in color from off-white to light yellow or beige. Its appearance can be influenced by various factors such as purity and specific synthesis methods.

Comment on solubility

Solubility of 3-(1-butylpyrrolidin-2-yl)-1H-indole

The solubility of 3-(1-butylpyrrolidin-2-yl)-1H-indole can be influenced by several factors, leading to variable outcomes in different environments. Here are some key aspects to consider:

  • Polarity: The presence of both hydrophobic (non-polar) and hydrophilic (polar) components in its structure suggests that 3-(1-butylpyrrolidin-2-yl)-1H-indole may exhibit moderate solubility in polar solvents, particularly those that can hydrogen bond.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents like ethanol and dimethyl sulfoxide (DMSO) than in water due to its hydrophobic characteristics.
  • Concentration: Solubility may vary with concentration, with the potential for higher solubility at elevated temperatures.

In general, while this compound may dissolve adequately in suitable organic solvents, its solubility in water is likely to be limited. Thus, careful consideration of the solvent choice is crucial for applications involving 3-(1-butylpyrrolidin-2-yl)-1H-indole.

Interesting facts

Interesting Facts about 3-(1-butylpyrrolidin-2-yl)-1H-indole

3-(1-butylpyrrolidin-2-yl)-1H-indole is a fascinating compound that bridges the gap between organic chemistry and medicinal applications. Here are some intriguing insights about this compound:

  • Structural Complexity: This compound features a unique blend of indole and pyrrolidine moieties, showcasing an impressive structural diversity that can lead to unique chemical properties.
  • Pharmacological Potential: The indole scaffold is common in many biologically active molecules, making this compound a candidate for evaluating various pharmacological effects.
  • Research Applications: Due to its distinctive structure, this compound is often studied for its anti-inflammatory and analgesic properties, providing insights into possible drug development.
  • Natural Occurrence: Indole derivatives have been found in numerous natural products, hinting at the compound's potential role in complex biological systems.
  • Synthesis Challenges: The synthesis of 3-(1-butylpyrrolidin-2-yl)-1H-indole poses unique challenges, requiring advanced techniques to ensure high yields and purity.
  • Interdisciplinary Interest: From organic chemists to pharmacologists, this compound attracts attention across various disciplines, highlighting the interplay between chemistry and biology.

As celebrated chemist Robert H. Grubbs once said, "The beauty of chemistry lies in exploring possibilities, where every compound opens the door to new realms of understanding." 3-(1-butylpyrrolidin-2-yl)-1H-indole is an excellent example of this beauty, embodying both complexity and potential in the vast world of chemical compounds.