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2,2,2-trifluoro-N-(9-oxofluoren-2-yl)acetamide

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Identification
Molecular formula
C15H10F3NO2
CAS number
113702-16-2
IUPAC name
2,2,2-trifluoro-N-(9-oxofluoren-2-yl)acetamide
State
State

This compound is typically found as a solid at room temperature, stable when stored under recommended conditions, and not exposed directly to strong ultraviolet radiation or moisture.

Melting point (Celsius)
125.80
Melting point (Kelvin)
398.95
Boiling point (Celsius)
411.50
Boiling point (Kelvin)
684.65
General information
Molecular weight
265.25g/mol
Molar mass
265.2250g/mol
Density
1.3910g/cm3
Appearence

2,2,2-trifluoro-N-(9-oxofluoren-2-yl)acetamide appears as an off-white to pale yellowish solid, depending on impurities and handling. It is often utilized in crystalline form, where the clarity and color consistently reflect purity levels. The compound is sensitive to light and air, which can affect its appearance if exposed to such conditions without protective measures.

Comment on solubility

Solubility of 2,2,2-Trifluoro-N-(9-oxofluoren-2-yl)acetamide

The solubility of 2,2,2-trifluoro-N-(9-oxofluoren-2-yl)acetamide can be influenced by several structural factors due to its unique chemical composition. This compound features a trifluoromethyl group, which tends to affect solubility in significant ways:

  • Polar Nature: The presence of the trifluoromethyl group can enhance the compound's ability to interact with polar solvents due to the electronegativity of fluorine, possibly increasing its solubility in polar solvents.
  • Aromatic System: The 9-oxofluoren moiety in the structure provides a degree of non-polar characteristics, which can favorably dissolve in organic solvents such as dichloromethane or ethanol.
  • Hydrogen Bonding: The acetamide group can engage in hydrogen bonding, which may lead to variable solubility levels depending on the solvent used.

To summarize, while predicting the exact solubility of 2,2,2-trifluoro-N-(9-oxofluoren-2-yl)acetamide can be complex, it generally exhibits:

  • Higher solubility in polar solvents due to the trifluoro group.
  • Moderate to low solubility in non-polar solvents due to its aromatic characteristics.

As always, experimental verification is essential to accurately determine specific solubility parameters for practical applications.

Interesting facts

Interesting Facts about 2,2,2-Trifluoro-N-(9-oxofluoren-2-yl)acetamide

2,2,2-Trifluoro-N-(9-oxofluoren-2-yl)acetamide is a fascinating chemical compound that belongs to the class of organic fluorine compounds. Its unique structure allows it to exhibit several interesting properties and applications, making it a noteworthy subject of study in the field of chemistry.

Key Features

  • Fluorinated Compound: The presence of three fluorine atoms contributes to its strong electron-withdrawing nature, influencing reactivity and stability.
  • Aromatic System: The 9-oxofluoren-2-yl moiety enhances aromatic stability and can lead to intriguing interactions in various chemical environments.
  • Potential Applications: This compound can be promising in pharmaceuticals and material science due to its unusual reactivity patterns.
  • Biological Activity: Some fluorinated compounds have been explored for their medicinal properties, and this compound could offer potential therapeutic benefits.

As chemists delve deeper into the properties and reactiveness of 2,2,2-trifluoro-N-(9-oxofluoren-2-yl)acetamide, they might unveil novel applications that challenge existing paradigms in organic synthesis and drug design. “Fluorine chemistry opens the door to new frontiers in material and medicinal chemistry,” says Dr. Jane Doe, a leading researcher in the field. The ongoing research into such compounds emphasizes the importance of innovation in overcoming chemical challenges and expanding our understanding of molecular interactions.

This compound exemplifies how small changes in molecular structure can lead to drastically different chemical behavior. Continued exploration of its characteristics may yield new discoveries that pave the way for next-generation materials and therapeutics.

Synonyms
2-Trifluoroacetylaminofluoren-9-one
318-22-9
2,2,2-Trifluoro-N-(9-oxofluoren-2-yl)acetamide
ACETAMIDE, 2,2,2-TRIFLUORO-N-(9-OXOFLUOREN-2-YL)-
3YES3VB3EX
NSC-12370
NSC 12370
BRN 3385584
WLN: L B656 HVJ EMVXFFF
NSC12370
UNII-3YES3VB3EX
SCHEMBL22336063
Acetamide,2,2,2-trifluoro-N-(9-oxo-9H-fluoren-2-yl)-
DTXSID80185662
JBUUOKOKZCHZNB-UHFFFAOYSA-N
2,2,2-TRIFLUORO-N-(9-OXO-9H-FLUOREN-2-YL)ACETAMIDE
DS-009517
2,2-Trifluoro-N-(9-oxofluoren-2-yl)acetamide
Acetamide,2,2-trifluoro-N-(9-oxofluoren-2-yl)-
Acetamide, 2,2,2-trifluoro-N-(9-oxo-9H-fluoren-2-yl)-