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Bifemelane

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Identification
Molecular formula
C16H24FN
CAS number
475-56-9
IUPAC name
N-[2-(4-fluorophenyl)ethyl]-1,7,7-trimethyl-norbornan-2-amine
State
State

Bifemelane is typically a solid at room temperature. It is often formulated into pharmaceutical forms for medical use.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
269.85
Boiling point (Kelvin)
543.00
General information
Molecular weight
243.36g/mol
Molar mass
243.3640g/mol
Density
1.0357g/cm3
Appearence

Bifemelane typically appears as a white or off-white crystalline solid. It is often provided as a powder or in tablet form for its pharmaceutically active formulations.

Comment on solubility

Solubility of N-[2-(4-fluorophenyl)ethyl]-1,7,7-trimethyl-norbornan-2-amine

The solubility of N-[2-(4-fluorophenyl)ethyl]-1,7,7-trimethyl-norbornan-2-amine can be influenced by several factors. As a complex organic compound, its solubility characteristics are dictated by its unique molecular structure and functional groups. Here are some key points to consider:

  • Polarity: The presence of a fluorophenyl group may enhance the compound's polarity, influencing its solubility in polar solvents.
  • Hydrogen Bonding: If the molecule has the capability to form hydrogen bonds, it may increase solubility in water or alcohols.
  • Solvent Interaction: This compound is likely to exhibit higher solubility in organic solvents, such as dichloromethane or ethyl acetate, owing to its hydrophobic parts.

It is important to note that solubility can vary greatly depending on temperature and the presence of other solutes or solvents. As with many organic compounds, various experimental conditions should be optimized to determine the exact solubility profile:

  • Temperature: An increase in temperature typically results in increased solubility for many organic compounds.
  • pH Levels: Acidic or basic environments can significantly alter the solubility, especially for amines.

In conclusion, the solubility of N-[2-(4-fluorophenyl)ethyl]-1,7,7-trimethyl-norbornan-2-amine is a multifaceted aspect influenced by its structural properties and the surrounding conditions. As emphasized in solubility studies, "understanding the solubility behavior of compounds is crucial for their practical application in pharmaceuticals and materials science."

Interesting facts

Interesting Facts about N-[2-(4-fluorophenyl)ethyl]-1,7,7-trimethyl-norbornan-2-amine

N-[2-(4-fluorophenyl)ethyl]-1,7,7-trimethyl-norbornan-2-amine, often referred to in scientific circles as a complex organic compound, has garnered attention for its unique structural features and potential applications. Here are some fascinating insights:

  • Structural Complexity: This compound showcases a distinctive bicyclic structure, characteristic of norbornan derivatives. Its fusion of a fluorophenyl group contributes to interesting electronic properties.
  • Pharmacological Potential: Compounds of this class are often studied in medicinal chemistry for their possible effects on neurotransmitter systems. Enhanced binding affinity can lead to promising therapeutic outcomes.
  • Fluorine's Impact: The presence of fluorine often enhances the metabolic stability of the compound, making it a hot topic in the development of pharmaceuticals. This halide can influence solubility and bioavailability, crucial factors in drug design.
  • Intriguing Applications: Researchers are exploring this compound in fields ranging from neuropharmacology to material sciences due to its unique properties. Its application could extend to developing new types of sensors or catalysts!

As a note, studying such compounds emphasizes the intricate relationship between structure and function, encouraging chemists to consistently explore new avenues. As Dr. Marie Curie once said, "One never notices what has been done; one can only see what remains to be done." The journey to uncovering the full potential of compounds like N-[2-(4-fluorophenyl)ethyl]-1,7,7-trimethyl-norbornan-2-amine is ongoing and exciting!

Synonyms
AKOS009005833