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Dibenzothiophene 2-phenyl ketone

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Identification
Molecular formula
C20H11F3OS
CAS number
19611-77-7
IUPAC name
dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone
State
State

At room temperature, Dibenzothiophene 2-phenyl ketone is in a solid state. It generally remains stable under standard laboratory conditions, making it suitable for various chemical applications and syntheses. Its stability is integral to its use in organic synthesis and material science research.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
454.50
Boiling point (Kelvin)
727.65
General information
Molecular weight
332.36g/mol
Molar mass
332.3590g/mol
Density
1.3700g/cm3
Appearence

Dibenzothiophene 2-phenyl ketone typically appears as a solid crystalline powder. This compound is characterized by its white to light yellow coloration, indicating its purity and specific structural properties. The crystalline form is often used for analytical and research purposes due to its defined structural and physical attributes.

Comment on solubility

Solubility of Dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone

Dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone, a compound characterized by its complex structure, exhibits distinctive solubility properties. The solubility of this compound can be influenced by various factors:

  • Polarity: Its structural framework suggests a relatively non-polar character due to the presence of multiple aromatic systems and trifluoromethyl groups that lower overall polarity.
  • Solvent Choice: This compound is more likely to dissolve in organic solvents such as chloroform, ethyl acetate, or benzene, compared to polar solvents like water.
  • Temperature Effects: Solubility can increase with temperature, a common behavior observed in many organic compounds.
  • Concentration Factors: At higher concentrations, the tendency to precipitate may increase, as solute molecules may reach saturation limits.

In summary, the solubility of dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone is predominantly influenced by its non-polar characteristics, favoring organic solvents over aqueous solutions. As stated, "Like dissolves like," hence the emphasis on selecting the right solvent system for optimal solubility outcomes.

Interesting facts

Exploring Dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone

Dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone, often referred to in shorthand as DBT-CF3, is an intriguing compound that showcases the fascinating intersections of organic chemistry and materials science. Here are several noteworthy aspects of this compound:

  • Structural Uniqueness: The compound features a dibenzothiophene core, which is a polycyclic aromatic compound known for its stability and unique electronic characteristics. The addition of a trifluoromethyl group enhances its electron-withdrawing properties, making it particularly interesting for various applications.
  • Applications in Materials Science: Due to its electronic properties, DBT-CF3 is being researched for use in organic light-emitting diodes (OLEDs) and organic photovoltaic devices. The incorporation of such compounds can influence the efficiency and stability of these technologies.
  • Environmental Considerations: Compounds like DBT-CF3 may have implications in environmental chemistry. The behavior of fluorinated compounds in ecosystems is a crucial area of research, especially regarding their persistence and accumulation in environmental matrices.
  • Pharmacological Potential: The structural features of dibenzothiophenes have piqued the interest of medicinal chemists. Some derivatives exhibit biological activity, suggesting that DBT-CF3 could potentially be explored for pharmaceutical applications.
  • Historical Context: Dibenzothiophene derivatives have historically been part of research into coal tar and petroleum products, playing a role in understanding the complex chemistry of fossil fuels and their derivatives.

In summary, dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone exemplifies the richness of organic compounds and their far-reaching potential across scientific disciplines. From materials science innovations to environmental monitoring, the study of such compounds opens up avenues for future research and development.

Synonyms
DIBENZOTHIOPHENE, 2-(m-TRIFLUOROMETHYLBENZOYL)-
2-(m-Trifluoromethylbenzoyl)dibenzothiophene
17739-81-0
DTXSID80170295
DTXCID6092786
dibenzothiophen-2-yl-[3-(trifluoromethyl)phenyl]methanone
BUSWROKLCOZQHR-UHFFFAOYSA-N