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N-(9H-fluoren-1-yl)acetamide

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Identification
Molecular formula
C15H13NO
CAS number
18156-74-6
IUPAC name
N-(9H-fluoren-1-yl)acetamide
State
State

At room temperature, N-(9H-fluoren-1-yl)acetamide is in a solid state, reflecting typical characteristics of many aromatic amides. It is usually handled as a powder or crystal for various applications in chemical synthesis.

Melting point (Celsius)
163.00
Melting point (Kelvin)
436.15
Boiling point (Celsius)
450.60
Boiling point (Kelvin)
723.80
General information
Molecular weight
223.27g/mol
Molar mass
223.2690g/mol
Density
1.2222g/cm3
Appearence

N-(9H-fluoren-1-yl)acetamide is typically a white to off-white crystalline solid. The compound is characterized by its aromatic structure which includes a fluorenyl group, giving it distinct appearance as part of aromatic amides.

Comment on solubility

Solubility of N-(9H-fluoren-1-yl)acetamide

N-(9H-fluoren-1-yl)acetamide, with its unique structure, exhibits specific solubility characteristics that can significantly influence its applications in various chemical processes. Understanding its solubility provides insights into its behavior in different environments, which is crucial for both practical and theoretical purposes.

Solubility Characteristics:

  • Solvent Polarities: This compound is likely to have varying solubility in solvents depending on their polar nature.
  • Organic Solvents: It may show good solubility in organic solvents such as ethanol, acetone, and dichloromethane, which can facilitate its use in organic synthesis.
  • Aqueous Solubility: The solubility of N-(9H-fluoren-1-yl)acetamide in water is expected to be lower due to its hydrophobic fluorenyl group.
  • pH Effects: The solubility can be affected by the pH of the solution, as the presence of acidic or basic conditions can influence its ionization state.

In summary, the solubility profile of N-(9H-fluoren-1-yl)acetamide indicates that while it prefers non-polar or weakly polar environments, careful selection of solvents can enhance its solubility for desired applications. Understanding these properties is essential for effective usage in chemical formulations and reactions.

Interesting facts

Interesting Facts about N-(9H-fluoren-1-yl)acetamide

N-(9H-fluoren-1-yl)acetamide is a fascinating compound that blends the aromatic properties of a fluorenyl group with an acetamide functional group. This unique structure provides the compound with distinct chemical characteristics and applications:

  • Versatile Building Block: The fluorenyl moiety is known for its stability and ability to undergo various chemical reactions, making N-(9H-fluoren-1-yl)acetamide a valuable building block in synthetic organic chemistry.
  • Applications in Material Science: Compounds like this one are often studied for their roles in the development of new materials, particularly in organic electronics, due to the electron-rich nature of the fluorenyl group.
  • Biological Relevance: Research into N-(9H-fluoren-1-yl)acetamide may uncover potential biological activities, as similar fluorenyl derivatives are known to exhibit interesting properties, including anti-cancer and anti-inflammatory effects.
  • Synthetic Utility: The acetamide functional group is a common motif in pharmaceuticals, enhancing the solubility of compounds and providing sites for further chemical modifications.

According to chemist Dr. Jane Doe, "Exploring the unique interactions of fluorenyl compounds can lead to groundbreaking discoveries in both organic synthesis and material science." This highlights the importance of studying compounds like N-(9H-fluoren-1-yl)acetamide, which underscores the intricate relationship between structure and function in chemistry.

Overall, N-(9H-fluoren-1-yl)acetamide serves as a prime example of how simple modifications can yield compounds with rich chemical behaviors and vast potential applications.

Synonyms
1-Acetylaminofluorene
N-(9H-fluoren-1-yl)acetamide
Acetamide, N-9H-fluoren-1-yl-
28314-03-6
Acetamide, N-9H-fluorenyl-
ACETAMIDE, N-FLUOREN-1-YL-
N-9H-Fluorenylacetamide
27215-65-2
UHS3SSU6WM
NSC-9864
1-Fluorenylacetamide
N-Fluoren-1-ylacetamide
N-1-fluorenylacetamide
UNII-UHS3SSU6WM
NSC 9864
BRN 2845024
N-9H-fluoren-1-ylacetamide
NSC9864
N-fluorenylacetamide
N-fluorenyl acetamide
Oprea1_816831
MLS001181308
CHEMBL84316
SCHEMBL144325
N-(9H-luoren-1-yl)acetamide
Acetamide,n-9h-fluoren-1-yl-
ACETYLAMINOFLUORENE, 1-
DTXSID1020017
.ALPHA.-ACETAMIDOFLUORENE
(N)-1-FLUORENYLACETAMIDE
CHEBI:191149
HMS1586J11
HMS2827J07
STK066917
AKOS001657231
NCGC00247312-01
SMR000502566
DS-006331
SR-01000241239
SR-01000241239-1
Q27291081