Skip to main content

(4-Chlorophenyl)(dibenzothiophen-3-yl)methanone

ADVERTISEMENT
Identification
Molecular formula
C19H11ClOS
CAS number
112701-89-0
IUPAC name
(4-chlorophenyl)-dibenzothiophen-3-yl-methanone
State
State
Solid at room temperature.
Melting point (Celsius)
181.00
Melting point (Kelvin)
454.00
Boiling point (Celsius)
481.00
Boiling point (Kelvin)
754.00
General information
Molecular weight
308.80g/mol
Molar mass
308.8000g/mol
Density
1.3500g/cm3
Appearence
Solid crystalline structure, typically appearing as white or off-white crystals or powder.
Comment on solubility

Solubility of (4-chlorophenyl)-dibenzothiophen-3-yl-methanone

The solubility of the compound (4-chlorophenyl)-dibenzothiophen-3-yl-methanone can be intriguing due to its structural characteristics. Understanding its solubility involves considering several factors:

  • Polarity: The presence of the chlorophenyl group may increase the compound's polarity, possibly leading to better solubility in polar solvents.
  • Functional Groups: The dibenzothiophen moiety is largely hydrophobic, which can hinder solubility in water but enhance solubility in organic solvents.
  • Temperature Effects: Typically, increasing temperature may improve the solubility of organic compounds, leading to greater dissolution in suitable solvents.

It is generally observed that:

  1. Compounds containing both polar and non-polar characteristics often show variable solubility depending on the solvent.
  2. This compound may exhibit limited solubility in water but could be more soluble in organic solvents such as ethanol or acetone.

As a final note, while the specific solubility data for (4-chlorophenyl)-dibenzothiophen-3-yl-methanone may not be extensively documented, experimentation in laboratory settings can provide valuable insights into its behavior in various solvents. Always remember the golden rule of solubility: “Like dissolves like.”

Interesting facts

Interesting Facts About (4-chlorophenyl)-dibenzothiophen-3-yl-methanone

(4-chlorophenyl)-dibenzothiophen-3-yl-methanone, often simply referred to as a derivative of dibenzothiophene, is a fascinating compound with unique applications and properties. Here are some noteworthy highlights:

  • Structural Complexity: This compound features a highly complex structure that includes both aromatic and heterocyclic components, which enhances its potential for interaction with biological systems.
  • Applications in Pharmaceuticals: Compounds derived from dibenzothiophene frameworks have shown promise in medicinal chemistry, particularly in developing anti-cancer agents and anti-inflammatory drugs.
  • Environmental Significance: The presence of sulfur in its structure raises interesting discussions about its behavior in environmental contexts, especially in relation to polycyclic aromatic hydrocarbons, which are known for their persistence and potential toxicity.
  • Research and Development: Continuous research is being conducted to explore novel derivatives of this compound, aiming to enhance their efficacy and reduce side effects.
  • Ethical Considerations: As with many compounds used in pharmacology, ethical considerations regarding the testing and use of such substances in humans and the environment are of prime importance.

This compound's intricate structure and potential applications make it a subject of interest in various fields, including organic chemistry, pharmacology, and environmental science. As we continue to investigate its properties and impacts, (4-chlorophenyl)-dibenzothiophen-3-yl-methanone exemplifies the exciting challenges and opportunities faced by chemists today.

Synonyms
17739-80-9
2-(p-Chlorobenzoyl)dibenzothiophene-
BRN 1583730
KETONE, p-CHLOROPHENYL 2-DIBENZOTHIENYL
p-Chlorophenyl dibenzothien-2-yl ketone
DTXSID20170294
5-17-10-00730 (Beilstein Handbook Reference)
DTXCID1092785
p-Chlorophenyl(dibenzothiophen-2-yl) ketone
(4-chlorophenyl)-dibenzothiophen-3-ylmethanone
3-(p-chlorobenzoyl)dibenzothiophene