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4-Fluoroamphetamine

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Identification
Molecular formula
C19H26BrFN
CAS number
372-75-8
IUPAC name
3-(4-fluorophenyl)propyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;bromide
State
State

At room temperature, 4-Fluoroamphetamine is typically in a solid state. Its crystalline form makes it easily identifiable among other substances of similar use.

Melting point (Celsius)
154.00
Melting point (Kelvin)
427.15
Boiling point (Celsius)
205.00
Boiling point (Kelvin)
478.15
General information
Molecular weight
319.26g/mol
Molar mass
319.2610g/mol
Density
1.2060g/cm3
Appearence

The compound appears as a white crystalline solid. It is often found in powder form and has no distinct odor.

Comment on solubility

Solubility of 3-(4-fluorophenyl)propyl-(1,7,7-trimethylnorbornan-2-yl)ammonium bromide

The solubility of 3-(4-fluorophenyl)propyl-(1,7,7-trimethylnorbornan-2-yl)ammonium bromide is influenced by various factors, including its ionic nature and molecular structure. Being a quaternary ammonium salt, its solubility characteristics can be summarized as follows:

  • Solvent Type: This compound is more soluble in polar solvents such as water and alcohols due to its ionic bromide component.
  • Temperature Dependence: The solubility generally increases with temperature, making higher temperatures more favorable for dissolving the compound.
  • pH Influence: The solubility can be affected by the pH of the solution, as variations can alter the ionization state of the compound.

In many cases, quaternary ammonium salts exhibit favorable solubility properties, making them valuable in various chemical applications. However, it's essential to note that while "solubility can vary under different conditions," 3-(4-fluorophenyl)propyl-(1,7,7-trimethylnorbornan-2-yl)ammonium bromide demonstrates a tendency for good solubility in suitable solvents, which opens avenues for further exploration in practical uses.

Interesting facts

Interesting Facts about 3-(4-fluorophenyl)propyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Bromide

This unique compound is recognized for its intricate structure and potential applications in various fields, particularly in medicinal chemistry and organic synthesis. Here are some fascinating aspects of this compound:

  • Pharmacological Potential: Compounds with ammonium functionalities often exhibit interesting biological activities, making them suitable candidates for drug discovery.
  • Structure Activity Relationship: The presence of a 4-fluorophenyl group can significantly influence the compound's interaction with biological targets, enhancing its potency or specificity.
  • Chirality and Asymmetry: The compound possesses chirality due to its multi-substituted backbone structure, which could lead to various stereoisomers, each with distinct properties.
  • Possible Applications: Beyond its medicinal potential, this compound can also be explored in material sciences, especially in the design of ion-conducting materials or sensors.
  • Research Significance: Such compounds are often subjects of studies aimed at understanding receptor interactions or mechanisms of action in a biological context.

In summary, 3-(4-fluorophenyl)propyl-(1,7,7-trimethylnorbornan-2-yl)ammonium bromide presents a rich avenue for research and application, reflecting the complexities and possibilities inherent in organic compounds. As emphasized by many chemists, "The true value of a compound lies beyond its molecular structure; it is in the potential it holds for innovation and discovery."

Synonyms
(+-)-endo-N-(3-(p-Fluorophenyl)propyl)-2-bornanamine hydrobromide
24629-72-9
2-BORNANAMINE, N-(3-(p-FLUOROPHENYL)PROPYL)-, HYDROBROMIDE, endo-(+-)-
RefChem:256675