Skip to main content

Carbamazepine

ADVERTISEMENT
Identification
Molecular formula
C15H12N2O
CAS number
298-46-4
IUPAC name
9-[2-(diethylamino)ethyl]-6-methyl-3,4-dihydro-2H-carbazol-1-one
State
State
solid at room temperature.
Melting point (Celsius)
189.00
Melting point (Kelvin)
462.15
Boiling point (Celsius)
431.70
Boiling point (Kelvin)
704.90
General information
Molecular weight
236.27g/mol
Molar mass
236.2680g/mol
Density
1.2805g/cm3
Appearence

Carbamazepine appears as a white to off-white crystalline powder. It is practically odorless and has a slightly bitter taste.

Comment on solubility

Solubility of 9-[2-(diethylamino)ethyl]-6-methyl-3,4-dihydro-2H-carbazol-1-one

The solubility of 9-[2-(diethylamino)ethyl]-6-methyl-3,4-dihydro-2H-carbazol-1-one in various solvents is influenced by its structure, particularly the presence of the diethylamino group and the carbazole moiety.

Key Points on Solubility:

  • Polar vs. Non-Polar Solvents: This compound, with its diethylamino functional group, suggests that it may exhibit higher solubility in polar solvents such as water or alcohol due to hydrogen bonding.
  • Temperature Effects: Like many organic compounds, its solubility can be temperature-dependent, often increasing with temperature.
  • Concentration Considerations: At higher concentrations, precipitation may occur, altering the apparent solubility of the compound.
  • pH Influence: The ionization state of the diethylamino group in varying pH environments can significantly affect solubility, enhancing it in acidic conditions.

In conclusion, while the diethylamino group generally enhances solubility in polar environments, the overall solubility profile of 9-[2-(diethylamino)ethyl]-6-methyl-3,4-dihydro-2H-carbazol-1-one warrants experimental investigation to confirm its behavior in various solvents under controlled conditions.

Interesting facts

Interesting Facts about 9-[2-(diethylamino)ethyl]-6-methyl-3,4-dihydro-2H-carbazol-1-one

9-[2-(diethylamino)ethyl]-6-methyl-3,4-dihydro-2H-carbazol-1-one is a fascinating compound primarily studied for its intriguing properties and potential applications in various fields. Below are some noteworthy aspects:

  • Biological Activity: This compound is of great interest in medicinal chemistry due to its potential bioactive properties. It is explored for its neuroprotective and anti-cancer activities, making it a subject of various pharmacological studies.
  • Structure and Function: The compound features a carbazole backbone, which is significant because carbazoles are known for their diverse biological activities. The diethylamino group is appended to the structure, enhancing its reactivity and interaction with biological targets.
  • Research Potential: Its unique chemical structure allows chemists to investigate derivatives of this compound that could lead to the development of new therapeutics. Research in synthetic modifications can expand its utility.
  • Application in Materials Science: Beyond pharmacology, compounds with similar structures are often explored in materials science for the development of organic semiconductors, dyes, and sensors.
  • Historical Context: The exploration of carbazole derivatives gained momentum in the mid-20th century, showcasing the evolution of synthetic methods that enable the preparation of such complex molecules.

In summary, 9-[2-(diethylamino)ethyl]-6-methyl-3,4-dihydro-2H-carbazol-1-one exemplifies the intersection of organic chemistry and pharmacology. As research advances, it remains to be seen how its intriguing properties can be leveraged to address current scientific challenges.