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Fluorenylacetamide

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Identification
Molecular formula
C21H16FNO
CAS number
93515-00-5
IUPAC name
N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide
State
State

At room temperature, this compound is in a solid state. It is stable under normal conditions but should be stored in a cool, dry place to prevent any degradation.

Melting point (Celsius)
315.60
Melting point (Kelvin)
588.75
Boiling point (Celsius)
555.30
Boiling point (Kelvin)
828.45
General information
Molecular weight
315.36g/mol
Molar mass
315.3450g/mol
Density
1.2460g/cm3
Appearence

N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide typically appears as a solid crystalline substance. The color can range from white to a pale yellow, depending on the purity and specific conditions during synthesis.

Comment on solubility

Solubility of N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide

The solubility of N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide can be influenced by various factors. As a compound with both aromatic and amine functionalities, its behavior in different solvents is quite intriguing.

  • Polar Solvents: This compound is likely to exhibit moderate solubility in polar solvents such as water and alcohols. The presence of the acetamide group may facilitate hydrogen bonding with polar solvent molecules.
  • Non-Polar Solvents: In non-polar solvents like hexane, solubility might be considerably low due to the compound's polar characteristics counteracting the non-polar nature of the solvent.
  • pH Sensitivity: The solubility could be affected by the pH of the solution, especially if protonation or deprotonation of the amine or amide functionalities occurs.

In summary, while general trends can be anticipated based on the functional groups present, the actual solubility will depend on specific experimental conditions and the solvent system used. As always, it is crucial to conduct solubility tests under controlled conditions to obtain precise data.

Interesting facts

Interesting Facts about N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide

N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide is a fascinating compound that captivates the interest of researchers and chemists alike. This compound is primarily notable for its distinct structural characteristics and functional applications. Here are some enlightening facts:

  • Innovative Potential: The incorporation of a 4-fluoroaniline group in its structure suggests promising biological activity. Fluorinated compounds often exhibit enhanced properties in medicinal chemistry, making this compound a candidate for pharmacological exploration.
  • Polymer Chemistry: Due to its unique aromatic structure, N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide could play a role in the development of advanced materials, including polymers with tailored properties.
  • Fluorine's Influence: The presence of fluorine in organic compounds can modify their electronic properties significantly. This can lead to improved stability and efficacy in various chemical reactions.
  • Research Applications: Scientists are often drawn to compounds like this for applications in drug design and development, where understanding the interactions at the molecular level is crucial for success.

In summary, N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide serves as a noteworthy example of how modifications in chemical structure can lead to enhanced properties and potential applications. Its unique combination of functional groups and stability due to fluorination opens up avenues for further research and innovation in various scientific fields.

As the famous chemist Dmitri Mendeleev once said, "There is nothing in this world that cannot be expressed in molecular terms," and compounds like N-[9-(4-fluoroanilino)-9H-fluoren-2-yl]acetamide illustrate the endless possibilities within the realm of chemistry.