Skip to main content

N-ethyl-3-phenyl-norbornan-2-amine

ADVERTISEMENT
Identification
Molecular formula
C17H23N
CAS number
946062-26-4
IUPAC name
N-ethyl-3-phenyl-norbornan-2-amine
State
State

Solid: N-ethyl-3-phenyl-norbornan-2-amine is solid at room temperature. This is typical of amines with similar molecular structures, which tend to crystallize and remain in solid form under ambient conditions.

Melting point (Celsius)
112.00
Melting point (Kelvin)
385.15
Boiling point (Celsius)
378.00
Boiling point (Kelvin)
651.15
General information
Molecular weight
241.37g/mol
Molar mass
241.3710g/mol
Density
1.0496g/cm3
Appearence

N-ethyl-3-phenyl-norbornan-2-amine is typically a crystalline solid. It may appear as a white or off-white powder, depending on the purity and specific preparation methods used. The crystalline structure can vary, influencing its texture and form.

Comment on solubility

Solubility of N-ethyl-3-phenyl-norbornan-2-amine

N-ethyl-3-phenyl-norbornan-2-amine is an intriguing compound when it comes to its solubility characteristics. This compound's ability to dissolve in various solvents can be influenced by several factors, including its molecular structure and the functional groups present.

Key points regarding the solubility of N-ethyl-3-phenyl-norbornan-2-amine include:

  • Polarity: The degree of polarity in molecules affects their solubility in polar versus non-polar solvents. N-ethyl-3-phenyl-norbornan-2-amine exhibits a certain level of polarity due to its amine group, which may allow for solubility in polar solvents like water.
  • Hydrogen Bonding: The presence of the amine functional group enables hydrogen bonding, which can further enhance solubility in aqueous environments.
  • Hydrophobic Character: The hydrophobic portions, such as the phenyl ring and the norbornane structure, may limit solubility in highly polar solvents. This dual nature can lead to complex solubility behavior.
  • Common Solvents: It is often soluble in organic solvents such as ethanol and acetone, while its solubility in water may be moderate.

In conclusion, while N-ethyl-3-phenyl-norbornan-2-amine displays interesting solubility traits derived from its structure and functional groups, one must evaluate specific conditions and solvent interactions to fully understand its behavior in different environments. Thus, it presents a fascinating subject for further investigation in fields such as organic chemistry and pharmacology.

Interesting facts

Interesting Facts about N-ethyl-3-phenyl-norbornan-2-amine

N-ethyl-3-phenyl-norbornan-2-amine is a fascinating organic compound that has gained attention in various fields of research, particularly in medicinal chemistry and organic synthesis. Here are some compelling facts that highlight its importance and uniqueness:

  • Structural Intrigue: The compound features a norbornane skeleton, which is characterized by its bicyclic structure. This unique architecture can influence its chemical properties and biological activity.
  • Potential Therapeutic Uses: Research suggests that amines like N-ethyl-3-phenyl-norbornan-2-amine may possess pharmacological properties. They could potentially act as intermediates in the synthesis of various pharmaceuticals, contributing to the development of new therapeutic agents.
  • Synthesis Challenges: The synthesis of N-ethyl-3-phenyl-norbornan-2-amine can be complex due to the stereochemistry associated with its norbornane framework. Chemists often utilize advanced techniques to control the formation of specific isomers, making it an intriguing challenge for synthetic chemists.
  • Neuroscience Exploration: Compounds similar to N-ethyl-3-phenyl-norbornan-2-amine are often explored for their effects on the nervous system. Investigating their potential as neuroprotective agents or cognitive enhancers remains a vital area of ongoing research.
  • Sustainable Chemistry: The study of such compounds aligns with the principles of green chemistry, as researchers seek to develop more sustainable synthetic methods that minimize waste and reduce environmental impact.

As researchers continue to explore the properties and applications of N-ethyl-3-phenyl-norbornan-2-amine, it holds the potential to contribute significantly to various scientific disciplines, paving the way for innovative advancements in chemistry and beyond.

Synonyms
Fencamfamin
Fencamfamine
Fencamfaminum
Euvitol
Fenacamfamin
Fencamfamina [DCIT]
phencamphamine
Fencanfamina
Fencamfamine [INN-French]
Fencamfaminum [INN-Latin]
Fencanfamina [INN-Spanish]
2-Ethylamino-3-phenylnorbornane
1209-98-9
3-Phenyl-N-ethyl-2-norbornanamine
2-NORBORNANAMINE, N-ETHYL-3-PHENYL-
2-Phenyl-3-ethylaminobicyclo(2.2.1)heptane
N-Ethyl-3-phenylbicyclo[2.2.1]heptan-2-amine
Bicyclo(2.2.1)heptan-2-amine, N-ethyl-3-phenyl-
Fencamfamina
Fencamfamin [INN:BAN]
Fencamfamin (INN)
UNII-NME1I5IGBK
Femcamfamine
DEA No. 1760
NME1I5IGBK
CHEMBL7010
SCHEMBL156977
DTXSID60862601
N06BA06
CHEBI:134895
IKFBPFGUINLYQI-UHFFFAOYSA-N
DB01463
NS00003664
D07343
N-Ethyl-3-phenylbicyclo[2.2.1]heptan-2-amine #
Q3742409