2-Phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline

Identification

Molecular formula

C₂₁H₂₆N₂

CAS number

77314-36-8

IUPAC name

2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline

State

At room temperature, 2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline is generally a liquid.

Melting point (Celsius)

72.00

Melting point (Kelvin)

345.15

Boiling point (Celsius)

340.00

Boiling point (Kelvin)

613.15

General information

Molecular weight

312.45g/mol

Molar mass

312.4740g/mol

Density

1.0900g/cm³

Appearence

The compound is typically a colorless to pale yellow liquid. It may crystallize under certain conditions, forming white or off-white crystalline solids.

Comment on solubility

Solubility of 2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline

2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline is an interesting compound with specific solubility characteristics that merit discussion. Generally, solubility can depend on various factors such as temperature, the solvent used, and the molecular structure of the compound itself. Here are some key points regarding its solubility:

Polar Solvents vs Non-polar Solvents: This compound is likely to be soluble in polar organic solvents due to the presence of polar functional groups in its structure, while its aromatic rings suggest some affinity for non-polar solvents as well.
Hydrophobic and Hydrophilic Interactions: The balance between the hydrophobic (water-repelling) phenyl and the hydrophilic (water-attracting) pyrrolidine group can affect solubility. Thus, it may exhibit selectivity in solubility depending on the solvent's characteristics.
Temperature Effects: Temperature changes can significantly impact solubility. Generally, increasing temperature can enhance the solubility of solid compounds in solvents.
pH Sensitivity: For compounds with amine groups, pH can also play a critical role. Changes in pH may lead to protonation or deprotonation, affecting solubility.

In summary, while specific solubility data for 2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline in various solvents might not be widely documented, its solubility is influenced by multiple factors such as solvent polarity, temperature, and pH conditions. Understanding these aspects is crucial for effectively utilizing this compound in various applications.

Interesting facts

Interesting Facts about 2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline

2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline is a unique chemical compound that has sparked interest in various fields of research and application. Here are some fascinating facts about this compound:

Structural Complexity: The compound consists of a phenyl ring combined with a pyrrolidine moiety, which enhances its structural diversity. This complexity often gives rise to interesting interactions and properties that can be explored in medicinal chemistry.
Pharmacological Potential: Due to its unique structure, 2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline has been studied for its potential pharmaceutical applications, particularly in the development of antidepressants and analgesics. Compounds that feature a pyrrolidine structure often exhibit significant biological activity.
Reactivity: The presence of the aniline group in the structure contributes to its reactivity, making it potential for various chemical syntheses, including new drug discovery and organic synthesis.
Research Interest: Scientists are particularly interested in studying the mechanisms of action of this compound, especially how modifications in its structure affect its biological activity.
Insights from Analogous Compounds: Compounds with similar structures have been shown to interact effectively with neurotransmitter systems in living organisms. This opens doors for understanding how variations in chemical structure can influence pharmacological effects.

Overall, 2-phenyl-N-(4-pyrrolidin-1-ylbutyl)aniline encapsulates the beauty and complexity of organic chemistry, presenting exciting opportunities for researchers and pharmaceutical scientists alike. Exploring such compounds not only enhances our knowledge of chemical interactions but also paves the way for new therapeutic advances.