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Fencamfamine hydrochloride

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Identification
Molecular formula
C16H26ClNO
CAS number
15686-37-2
IUPAC name
2-furylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

At room temperature, fencamfamine hydrochloride is a solid. It is stable under normal conditions but should be stored in a dry, cool place away from light and moisture to ensure its integrity.

Melting point (Celsius)
191.50
Melting point (Kelvin)
464.65
Boiling point (Celsius)
193.10
Boiling point (Kelvin)
466.25
General information
Molecular weight
282.83g/mol
Molar mass
282.8330g/mol
Density
1.0363g/cm3
Appearence

Fencamfamine hydrochloride typically appears as a white or almost white crystalline powder. It is visually characterized by its finely divided crystals that can often be compressed into tablets or incorporated into various pharmaceutical formulations.

Comment on solubility

Solubility of 2-furylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride

The solubility of the compound 2-furylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride can be investigated through several key points:

  • Polarity: The presence of a furyl group contributes to the overall polarity of the molecule, which can influence its interaction with polar solvents like water.
  • Temperature dependence: Solubility can significantly vary with temperature; typically, higher temperatures can enhance solubility for organic ammonium salts.
  • Hydration effects: The quaternary ammonium structure suggests that it may have strong interactions with water molecules, potentially leading to good solubility in aqueous solutions.
  • Comparative solubility: When pitting against similar compounds, this ammonium salt is likely to be more soluble in polar solvents compared to its less polar counterparts.

In summary, while the exact solubility profile of this compound requires empirical data for precise characterization, it is generally anticipated that 2-furylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride exhibits favorable solubility in polar solvents, particularly in the presence of factors such as temperature and ionic strength.

Interesting facts

Interesting Facts about 2-furylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride

The compound 2-furylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride is a fascinating example of organic chemistry that showcases the diverse potentials of ammonium salts. Here are some compelling insights:

  • Structural Complexity: The inclusion of the norbornane structure contributes to the compound's three-dimensional arrangement, making it intriguing for theoretical studies in stereochemistry.
  • Biological Relevance: Compounds related to ammonium salts often exhibit interesting biological activities, including their potential use as pharmacophores in medicinal chemistry.
  • Versatility in Synthesis: The synthetic pathways to create such complex structures can involve a variety of reaction mechanisms, including alkylation and functional group transformations, showcasing the versatility of organic synthesis techniques.
  • Potential Applications: This compound may represent a class of compounds suitable for research into drug development, as similar structures have been found to influence biological systems significantly.
  • Research Interest: Chemists are continually exploring the effects of substituents like the furylmethyl group, as they may enhance the compound's reactivity or solubility, opening up further research avenues.

In summary, 2-furylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride not only embodies intricate structural nuances but also holds the potential for significant scientific exploration, making it a noteworthy subject for further study in both organic chemistry and pharmacology.

Synonyms
(+-)-endo-N-2-Bornylfurfurylamine hydrochloride
FURFURYLAMINE, N-2-BORNYL-, HYDROCHLORIDE, endo-(+-)-
24629-71-8
RefChem:345868