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N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine

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Identification
Molecular formula
C18H18BrN
CAS number
802854-78-6
IUPAC name
N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine
State
State

This compound is a solid at room temperature.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
338.00
Boiling point (Kelvin)
611.15
General information
Molecular weight
326.24g/mol
Molar mass
326.2380g/mol
Density
1.3750g/cm3
Appearence

This compound is typically a crystalline solid with a pale color.

Comment on solubility

Solubility of N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine

N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine presents interesting solubility characteristics influenced by its molecular structure. The presence of various functional groups contributes to its solubility in certain solvents. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is likely to be more soluble in organic solvents such as chloroform, ether, and dichloromethane due to its hydrophobic fluorenyl core.
  • Water Solubility: The introduction of the bromopropyl and ethyl groups could create minor polar characteristics; nonetheless, solubility in water is expected to be limited. Generally, compounds with larger hydrophobic regions exhibit lower solubility in water.
  • Temperature Influence: Solubility can also be affected by temperature. Increasing the temperature often enhances solubility in many organic solvents, which may apply to this compound as well.

In conclusion, while N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine may show considerable solubility in non-polar solvents, it is anticipated to have limited solubility in polar solvents like water. As with many organic compounds, understanding the solubility profile is essential for practical applications and further research.

Interesting facts

Interesting Facts about N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine

N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine is a fascinating compound, primarily due to its unique chemical structure and the array of applications it holds in various fields. Here are some compelling aspects worth noting:

  • Versatile Intermediate: This compound serves as an important intermediate in the synthesis of other complex molecules. Its unique structure allows it to participate in a variety of chemical reactions, making it invaluable in organic synthesis.
  • Fluorene Derivative: The fluorene moiety in this compound not only impacts its chemical behavior but also enhances its physical properties. Fluorenes are known for their stability and contribute to the compound's overall robustness.
  • Potential Biological Activity: Researchers have begun to explore the biological implications of compounds like N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine. Preliminary studies suggest that it may exhibit interesting pharmacological activities, warranting further investigation.
  • Importance of Bromine: The presence of the bromine atom in the structure increases the compound's reactivity, making it a useful building block in the synthesis of pharmaceuticals and agrochemicals. Brominated compounds are often key players in medicinal chemistry.
  • Research Applications: As a result of its unique characteristics, this compound is frequently used in research laboratories for various studies, including materials science, biochemistry, and organic chemistry. It presents opportunities for discovering novel reactions and pathways.

In summary, N-(2-bromopropyl)-N-ethyl-9H-fluoren-9-amine is more than just a chemical entity; it embodies the intersection of diverse scientific disciplines, illustrating the complex beauty of chemistry. Whether in synthetic methods or potential therapeutic applications, the compound continues to pique the interest of chemists and researchers alike.