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4'-Fluoropropionanilide

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Identification
Molecular formula
C14H18FNO
CAS number
1484-13-5
IUPAC name
1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one
State
State
Typically, it is found in a solid state at room temperature. It is stable and does not easily transition to a gas despite its relatively high molecular weight.
Melting point (Celsius)
179.60
Melting point (Kelvin)
452.80
Boiling point (Celsius)
370.50
Boiling point (Kelvin)
643.60
General information
Molecular weight
221.30g/mol
Molar mass
221.2860g/mol
Density
1.1539g/cm3
Appearence

The compound typically appears as a white crystalline powder. It is relatively pure and does not have significant color variations. The texture is often described as fine and homogeneous.

Comment on solubility

Solubility of 1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one

The solubility of 1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one is an important factor to consider in its application and behavior in various environments. This compound, which contains both aromatic and aliphatic structures, exhibits unique solubility characteristics:

  • Polarity: Due to the presence of the piperidyl group, the compound may demonstrate some polar behavior, potentially increasing its solubility in polar solvents.
  • Solvent Compatibility: It is anticipated that 1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one will be more soluble in organic solvents like ethanol and methanol rather than water, given the hydrophobic aromatic characteristics.
  • Temperature Influence: The solubility may improve with increasing temperature, a common trend seen in many organic compounds.

In conclusion, while the precise solubility parameters of 1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one may require experimental determination, we can anticipate it to be more soluble in organic environments, affected by factors such as solvent type and temperature. Understanding these solubility aspects is crucial for effective handling and application in chemical processes.

Interesting facts

Interesting Facts about 1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one

This intriguing compound, known as 1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one, is categorized as a synthetic stimulant and has garnered attention in numerous scientific studies. Here are some compelling aspects of this compound:

  • Synthetic Origins: This compound is part of a class of chemicals that are purposefully synthesized for their psychoactive effects. It contains a piperidine moiety, which is often associated with various pharmacological activities.
  • Research Interest: Due to its structural similarity to other known stimulants, researchers are keen to study its effects and mechanism of action. It may provide insights into the pharmacology of psychoactive substances.
  • Fluorine Substitution: The presence of the fluorine atom in the aromatic ring enhances the compound's lipophilicity, which may influence its ability to cross biological membranes, potentially affecting its bioavailability and therapeutic applications.
  • Potential Applications: While still under investigation, this compound may hold promise in treating a variety of psychological conditions, including depression and ADHD. Stimulants often play a critical role in managing such disorders.
  • Legal Status: The legal status of this compound is complex and varies by region, highlighting the ongoing discussions about the regulation of synthetic drugs. Users and researchers must stay informed about the legislative environment surrounding it.

As science continues to evolve, so does the understanding of compounds like 1-(4-fluorophenyl)-3-(1-piperidyl)butan-1-one. “Every new discovery opens a door to understanding the vast landscape of chemical interactions.” Scientists hope that further exploration will reveal not just the safety profile of compounds like this but also their potential as therapeutic agents.