Skip to main content

N-Propyladamantan-1-amine

ADVERTISEMENT
Identification
Molecular formula
C13H23N
CAS number
7519-35-7
IUPAC name
N-propyladamantan-1-amine
State
State
Liquid at room temperature, should be handled carefully due to its chemical nature.
Melting point (Celsius)
43.50
Melting point (Kelvin)
316.65
Boiling point (Celsius)
259.30
Boiling point (Kelvin)
532.45
General information
Molecular weight
177.31g/mol
Molar mass
177.3080g/mol
Density
0.9923g/cm3
Appearence

N-Propyladamantan-1-amine is typically a colorless to pale-yellow liquid. It may appear slightly viscous and is often stored in glass containers due to its liquid nature.

Comment on solubility

Solubility of N-propyladamantan-1-amine

N-propyladamantan-1-amine, a compound characterized by its unique adamantane structure combined with an amine functional group, exhibits interesting solubility behavior. Understanding its solubility is essential for applications in pharmaceuticals and materials science.

Key Solubility Characteristics:

  • Polarity: The presence of the amine group suggests a certain degree of polarity, which can influence its solubility in polar solvents like water.
  • Hydrophobic Interaction: The adamantane core is notably hydrophobic, which may limit the compound's solubility in aqueous environments.
  • Organic Solvents: N-propyladamantan-1-amine is likely to be more soluble in non-polar organic solvents, such as hexane or chloroform, due to the hydrophobic nature of the adamantane framework.

As a result, one might summarize its solubility behavior with the phrase: "Highly soluble in organic solvents but poorly soluble in water." This dual behavior makes it a fascinating compound for studies related to solubility and compound interactions in different solvent environments.

Interesting facts

Interesting Facts about N-propyladamantan-1-amine

N-propyladamantan-1-amine is a fascinating compound that belongs to a unique class of chemicals known as adamantanes. This structure lends itself to a variety of interesting properties and potential applications. Here are some key points that highlight the significance of this compound:

  • Unique Structure: N-propyladamantan-1-amine features a core adamantane framework, which is a polycyclic compound characterized by a diamond-like structure composed of four fused cyclohexane rings. This unique arrangement contributes to its intriguing physical properties.
  • Biological Potential: Compounds with the adamantane structure have garnered attention in medicinal chemistry. For instance, derivatives of adamantane have been explored for use in antiviral therapies, showcasing their ability to interfere with various viral replication processes.
  • Drug Development: The presence of the amine functional group in N-propyladamantan-1-amine enhances its potential as a pharmacological agent. Amines are known for their ability to form hydrogen bonds, which can improve solubility and receptor binding in biological systems.
  • Hydrophobic Nature: The bulkiness of the adamantane structure often leads to hydrophobic interactions. This characteristic can be advantageous in designing compounds with specific interactions in biological membranes or in drug design to improve bioavailability.
  • Research Applications: Ongoing research continues to explore the parameters of N-propyladamantan-1-amine within organic synthesis and materials science, offering exciting prospects for future innovations.

As a compound that bridges various fields such as medicinal chemistry and materials science, N-propyladamantan-1-amine serves as a prime example of how structural characteristics can dictate a compound's behavior and application. Its potential is still being uncovered, making it a compound of interest for many scientists.

Synonyms
N-propyladamantan-1-amine
SCHEMBL60897
AKOS000227364
N-Propyladamantan-1-amine, AldrichCPR
Tricyclo[3.3.1.1]decan-1-amine, N-propyl-