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N-(9H-fluoren-4-yl)acetamide

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Identification
Molecular formula
C15H13NO
CAS number
5228-47-1
IUPAC name
N-(9H-fluoren-4-yl)acetamide
State
State

At room temperature, N-(9H-fluoren-4-yl)acetamide is typically a solid.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
422.00
Boiling point (Kelvin)
695.15
General information
Molecular weight
225.27g/mol
Molar mass
225.2690g/mol
Density
1.2500g/cm3
Appearence

It is usually a white to off-white crystalline solid. The compound appears as powdery crystals.

Comment on solubility

Solubility of N-(9H-fluoren-4-yl)acetamide

N-(9H-fluoren-4-yl)acetamide, a compound characterized by its unique structure, exhibits interesting solubility properties that are important for its applications in various chemical contexts. Here are some key points regarding its solubility:

  • Polarity: The presence of the acetamide functional group contributes to the polarity of the molecule, which can enhance its solubility in polar solvents.
  • Solvent Interaction: This compound tends to be more soluble in polar aprotic solvents like dimethyl sulfoxide (DMSO) or N,N-dimethylformamide (DMF) than in nonpolar solvents.
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, allowing for better dissolution in hot solvents.
  • Applications in Synthesis: The solubility characteristics of N-(9H-fluoren-4-yl)acetamide are critical in synthetic pathways where solvent choice impacts reaction rates and yields.

It is important to remember that solubility can be influenced by various factors such as pressure, concentration, and the presence of other solutes. Understanding these factors is essential for effectively utilizing N-(9H-fluoren-4-yl)acetamide in chemical applications.

Interesting facts

Interesting Facts about N-(9H-fluoren-4-yl)acetamide

N-(9H-fluoren-4-yl)acetamide is a fascinating compound that showcases the intersection of organic chemistry and material science. This compound has garnered attention for several reasons:

  • Fluorene Derivative: The backbone of this compound comes from fluorene, a polycyclic aromatic hydrocarbon known for its stability and interesting electronic properties.
  • Biological Relevance: Compounds like N-(9H-fluoren-4-yl)acetamide are often studied for their potential biological activity, particularly in medicinal chemistry, where they may exhibit interesting pharmacological properties.
  • Synthetic Versatility: The presence of the acetamide group makes it a valuable intermediate in organic synthesis, allowing for various functionalizations that can lead to diverse chemical libraries.
  • Application in Nanotechnology: Due to its unique structure, it is being explored in nanotechnology, especially in creating novel materials with enhanced electronic and optical properties.
  • Research Interest: This compound is a subject of ongoing research, with studies looking into its interactions with other molecules and its potential role in the development of new materials and drugs.

As scientists delve deeper into the properties of N-(9H-fluoren-4-yl)acetamide, they continue to uncover its potential applications ranging from organic electronics to advanced drug delivery systems. Its intriguing structure represents a bridge between traditional organic compounds and modern technological innovations, making it a valuable compound for both academic research and industrial applications.

In the words of a noted chemist, *“The true power of chemistry lies not just in what we discover, but in the potential of what we can create.”* With compounds like N-(9H-fluoren-4-yl)acetamide, that potential is both exciting and promising.

Synonyms
4-ACETYLAMINOFLUORENE
28322-02-3
4-Fluorenylacetamide
4-Acetylaminofluoren
N-Fluoren-4-ylacetamide
Acetamide, N-fluoren-4-yl-
N-4-Fluorenylacetamide
Acetamide, N-9H-fluoren-4-yl-
4-AAF
Acetamide, N-fluoren-4-yl
Acetamide, N-9H-fluoren-4-yl
U41BO8XU2Z
DTXSID1020019
CHEBI:76343
NSC-9866
RefChem:97636
DTXCID9019
248-964-3
4-Acetamidofluorene
N-(9H-Fluoren-4-yl)acetamide
N-9H-Fluoren-4-ylacetamide
NSC 9866
CCRIS 735
4-Acetylaminofluoren [German]
HSDB 4329
EINECS 248-964-3
UNII-U41BO8XU2Z
BRN 2975269
4AAF
SCHEMBL1273609
CHEMBL2311070
N-(9H-fluoren-4-yl)ethanamide
SCHEMBL30002207
NSC9866
4-ACETYLAMINOFLUORENE [HSDB]
AKOS015889873
DB-047377
NS00028458
ST50410763
A819413
Q27145900