Skip to main content

N'-(p-tolyl)naphthalene-1-carboxamidine

ADVERTISEMENT
Identification
Molecular formula
C18H16N2
CAS number
14284-60-7
IUPAC name
N'-(p-tolyl)naphthalene-1-carboxamidine
State
State

At room temperature, N'-(p-tolyl)naphthalene-1-carboxamidine is typically a solid. It does not readily dissolve in water, reflecting its primarily hydrophobic character due to the aromatic groups present in its structure.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
248.33g/mol
Molar mass
248.3270g/mol
Density
1.1987g/cm3
Appearence

N'-(p-tolyl)naphthalene-1-carboxamidine appears as a white crystalline solid. The structure typically includes a rigid and planar arrangement due to the naphthalene core, with a functional group that introduces some polarity.

Comment on solubility

Solubility of N'-(p-tolyl)naphthalene-1-carboxamidine

N'-(p-tolyl)naphthalene-1-carboxamidine presents intriguing solubility characteristics that are dependent on several factors. Due to its organic nature, its solubility can vary widely in different solvents.

  • Polar Solvents: Compounds similar to N'-(p-tolyl)naphthalene-1-carboxamidine often exhibit limited solubility in polar solvents such as water, due to their hydrophobic aromatic structures.
  • Non-Polar Solvents: This compound is more likely to dissolve in non-polar solvents (e.g., hexane or chloroform) where aromatic interactions can dominate, enhancing solubility.
  • Concentration: At higher concentrations, the solubility may marginally improve, but this is typically constrained by the inherent properties of the compound.

It's also important to consider that temperature plays a crucial role in solubilization; generally, higher temperatures can lead to increased solubility in organic solvents. As such, understanding the delicate balance of these properties is essential for practical applications, particularly in synthesis and formulation.

In conclusion, while N'-(p-tolyl)naphthalene-1-carboxamidine may not be highly soluble in polar media, its behavior in non-polar solvents offers valuable insights for chemists looking to manipulate its properties for various uses.

Interesting facts

Interesting Facts About N'-(p-tolyl)naphthalene-1-carboxamidine

N'-(p-tolyl)naphthalene-1-carboxamidine is a fascinating compound with multiple intriguing properties and potential applications. This compound exemplifies the complexities and versatility found within organic chemistry.

Chemical Structure and Characteristics

This compound features a naphthalene backbone, which is a polycyclic aromatic hydrocarbon. The presence of the p-tolyl (para-tolyl) group significantly influences its chemical behavior and reactivity. Here are some noteworthy points:

  • Amidine Functional Group: The amidine group present in the compound is known for its high basicity and nucleophilicity, making it a valuable motif in many synthetic transformations.
  • Benefits of Aromatic Rings: The aromatic nature of naphthalene contributes to its stability, allowing it to participate in various chemical reactions while maintaining structural integrity.
  • Substituent Effects: The addition of the p-tolyl group can affect the electronic distribution within the compound, potentially influencing its reactivity and interaction with other molecules.

Applications and Potential Uses

N'-(p-tolyl)naphthalene-1-carboxamidine holds promise in several fields:

  • Pharmaceutical Chemistry: With its unique functional groups, this compound might be a candidate for drug development, particularly in targeting specific biological pathways.
  • Material Science: The properties of naphthalene derivatives, including this compound, are being explored for use in advanced materials, such as organic semiconductors.
  • Research Applications: Scientists often utilize compounds like this in research to explore reaction mechanisms and to develop new methodologies in organic synthesis.

Conclusion

The intriguing structure and chemical properties of N'-(p-tolyl)naphthalene-1-carboxamidine showcase the rich diversity in the world of chemical compounds. With ongoing research, the full potential of this compound may be unveiled, leading to innovative applications across multiple domains.

Synonyms
1-NAPHTHAMIDINE, N-p-TOLYL-
N-p-Tolyl-1-naphthamidine
BRN 2849222
1-Naphthalenecarboximidamide, N-(4-methylphenyl)-
23564-93-4
DTXSID20178179
RefChem:232360
DTXCID00100670