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N-(9H-fluoren-3-yl)acetamide

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Identification
Molecular formula
C15H13NO
CAS number
3938-31-2
IUPAC name
N-(9H-fluoren-3-yl)acetamide
State
State

At room temperature, N-(9H-fluoren-3-yl)acetamide is in a solid state. It usually manifests in a crystalline form, making it relatively easy to handle in laboratory conditions.

Melting point (Celsius)
128.00
Melting point (Kelvin)
401.15
Boiling point (Celsius)
485.50
Boiling point (Kelvin)
758.65
General information
Molecular weight
225.27g/mol
Molar mass
225.2680g/mol
Density
1.2070g/cm3
Appearence

N-(9H-fluoren-3-yl)acetamide typically presents as a white to off-white crystalline solid. Its appearance may vary slightly based on its purity and the presence of any impurities.

Comment on solubility

Solubility of N-(9H-fluoren-3-yl)acetamide

N-(9H-fluoren-3-yl)acetamide, with its unique structure, exhibits interesting solubility characteristics that are noteworthy for researchers and professionals alike. Understanding the solubility of this compound is crucial for its application in various chemical processes.

Factors Influencing Solubility

The solubility of N-(9H-fluoren-3-yl)acetamide is influenced by several factors, including:

  • Polarity: The presence of the amide functional group contributes to the overall polarity of the molecule, affecting its interactions with solvents.
  • Hydrogen bonding: The ability to form hydrogen bonds increases its solubility in polar solvents.
  • Temperature: Generally, an increase in temperature enhances solubility, as more energy allows for better interaction with solvent molecules.

Solvent Compatibility

N-(9H-fluoren-3-yl)acetamide is expected to have varying solubility in different solvents:

  • Polar solvents: Likely soluble in water, methanol, and ethanol due to hydrogen bonding.
  • Nonpolar solvents: Limited solubility in hydrocarbons and nonpolar organic solvents.

In summary, the solubility of N-(9H-fluoren-3-yl)acetamide is a multifaceted aspect that combines polarity, hydrogen bonding, and environmental conditions. Understanding these factors can empower scientists to effectively utilize this compound in their respective fields. As expressed, "The key to dissolution is often in the nature of the bonds formed between solute and solvent." Thus, the exploration of this compound's solubility remains an engaging area of study.

Interesting facts

Interesting Facts About N-(9H-fluoren-3-yl)acetamide

N-(9H-fluoren-3-yl)acetamide is a fascinating compound that bridges organic chemistry with medicinal applications. This compound features a unique structure that includes the fluorenyl group, which is derived from fluorene, a polycyclic aromatic hydrocarbon known for its intriguing properties. Here are some key points that highlight the significance of N-(9H-fluoren-3-yl)acetamide:

  • Versatile Building Block: The fluorenyl moiety makes this compound an excellent building block in organic synthesis. Its ability to easily undergo chemical transformations allows chemists to create diverse derivatives for various applications.
  • Potential in Medicinal Chemistry: Compounds related to this structure have shown promise in biomedical research, particularly in the development of pharmaceuticals aimed at treating conditions like cancer and neurodegenerative diseases.
  • Research Applications: Its role as a reagent or probe in research makes N-(9H-fluoren-3-yl)acetamide valuable in studying enzyme mechanisms, binding affinities, and molecular interactions.
  • Fluorescent Properties: The conjugated system within the compound provides interesting photophysical properties, allowing it to be used in luminescent applications.

As a scientist or chemistry student, one might say, "N-(9H-fluoren-3-yl)acetamide embodies the spirit of innovation in organic chemistry." Its multifaceted nature demonstrates how simple modifications in molecular structure can lead to significant advancements in materials science and drug discovery.

In conclusion, this compound not only enriches our understanding of organic synthesis but also opens the door to new research opportunities. Its versatility, potential medicinal benefits, and engaging properties make it a subject worthy of further exploration.

Synonyms
N-3-Fluorenylacetamide
3-Acetylaminofluorene
3-Fluorenylacetamide
Acetamide, N-3-fluorenyl-
N-9H-Fluoren-3-ylacetamide
NSC 9865
UNII-4P9MD74D4T
BRN 2114187
NSC-9865
DTXSID40212125
4-12-00-03388 (Beilstein Handbook Reference)
DTXCID40134616
ccris 4222
N-Acetyl-3-aminofluorene
Acetamide, N-9H-fluoren-3-yl-
6292-55-3
ACETAMIDE, N-FLUOREN-3-YL-
4P9MD74D4T
CHEMBL84313
Acetamide, N-(2-fluorenyl)-
NSC9865
Q27260325
Z27570505