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N-(9H-Fluoren-2-yl)-2,2,2-trifluoroacetamide

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Identification
Molecular formula
C15H10F3NO
CAS number
24004-68-4
IUPAC name
N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide
State
State

At room temperature, N-(9H-Fluoren-2-yl)-2,2,2-trifluoroacetamide remains as a solid substance. It is stable under normal laboratory conditions, and does not readily evaporate or react with atmospheric components.

Melting point (Celsius)
176.50
Melting point (Kelvin)
449.70
Boiling point (Celsius)
417.50
Boiling point (Kelvin)
690.70
General information
Molecular weight
279.26g/mol
Molar mass
279.2630g/mol
Density
1.3589g/cm3
Appearence

The compound appears as a white crystalline solid under standard conditions. Its crystalline nature can be observed under a microscope, revealing its distinct lattice structure, common to organic crystalline compounds.

Comment on solubility

Solubility of N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide

N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is a compound that showcases unique solubility characteristics due to its molecular structure and the presence of multiple functional groups. Understanding the solubility of this compound is crucial for its applications in various chemical processes.

  • Polarity: The trifluoroacetamide group introduces notable polarity, which can affect solubility in polar solvents.
  • Solvent Interaction: This compound is likely to be more soluble in polar protic solvents (such as alcohols) compared to non-polar solvents, due to hydrogen bonding capabilities.
  • Temperature Dependency: Solubility may increase with temperature, which is a common characteristic of many organic compounds.
  • Special Considerations: The presence of fluorine atoms can enhance solubility in specific fluorinated solvents, making them ideal for specialized applications.

In summary, solubility of N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is influenced by its polarity, functional groups, and the nature of the solvent used. Understanding these factors is key for optimizing its use in different chemical environments.

Interesting facts

N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide

N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is a compound that showcases the fascinating interplay between organic chemistry and material science. Here are some intriguing facts that highlight its significance:

  • Fluorine Influence: The presence of fluorine atoms in this compound significantly alters its chemical properties. Fluorine is known for its electronegativity, which can influence the reactivity and stability of organic molecules.
  • Potential Applications: Compounds like N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide could have applications in various fields, such as:
    • Medicinal chemistry
    • Polymer science
    • Material fabrication
  • Synthesis and Reactions: Its synthesis involves amino chemistry, whereby functional groups are introduced to create complex molecules, making it an interesting compound for students studying organic synthesis.
  • Structure and Function Relationship: Understanding the relationship between the compound's structure and its anticipated properties can help researchers develop new materials with tailored functions for specific applications.

As stated by a renowned chemist, “The beauty of chemistry lies in its ability to create and manipulate molecules in innovative ways.” This compound exemplifies how careful design can lead to functional compounds that play critical roles in scientific advancements.

Overall, N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is not merely a chemical entity but a showcase of the vast possibilities within the realm of chemistry.

Synonyms
363-17-7
N-(2-Fluorenyl)-2,2,2-trifluoroacetamide
N-(9H-Fluoren-2-yl)-2,2,2-trifluoroacetamide
2-Trifluoroacetylaminofluorene
N-Fluoren-2-yl-2,2,2-trifluoroacetamide
2,2,2-Trifluoro-N-(fluoren-2-yl)acetamide
ACETAMIDE, N-FLUOREN-2-YL-2,2,2-TRIFLUORO-
N-9H-fluoren-2-yl-2,2,2-trifluoroacetamide
Acetamide, N-9H-fluoren-2-yl-2,2,2-trifluoro-
2-(2,2,2-Trifluoroacetamido)fluorene
DTXSID3020629
454X3J3CX8
NSC-12283
2-((Trifluoroacetyl)amino)fluorene
2-[(Trifluoroacetyl)amino]fluorene
NSC 12283
BRN 2814131
2-Aminofluorene, TFA
CHEMBL82129
DTXCID70629
UNII-454X3J3CX8
WLN: L B656 HHJ EMVXFFF
NSC12283
Tox21_301891
AKOS009038699
N-(2-Fluorenyl)-2,2-trifluoroacetamide
NCGC00255119-01
CAS-363-17-7
2,2-Trifluoro-N-(fluoren-2-yl)acetamide
DS-006332
NS00126685
Fluorenyl)-2,2,2-trifluoroacetamide, N-(2-
Acetamide,n-9h-fluoren-2-yl-2,2,2-trifluoro-
N-(9H-Fluoren-2-yl)-2,2,2-trifluoroacetamide #
Q63088208
632-237-6