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Naphtho[2,3-f]benzothiophene

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Identification
Molecular formula
C16H10S
CAS number
205-12-9
IUPAC name
naphtho[2,3-f]benzothiophene
State
State

At room temperature, naphtho[2,3-f]benzothiophene is typically found in a solid state. It is characterized by its crystalline form and is stable under normal conditions.

Melting point (Celsius)
106.00
Melting point (Kelvin)
379.15
Boiling point (Celsius)
426.00
Boiling point (Kelvin)
699.15
General information
Molecular weight
234.31g/mol
Molar mass
234.3110g/mol
Density
1.3100g/cm3
Appearence

Naphtho[2,3-f]benzothiophene typically appears as a pale yellow crystalline powder. It has a specific crystalline structure and can be visually identified by its distinctive color and form.

Comment on solubility

Solubility of Naphtho[2,3-f]benzothiophene

Naphtho[2,3-f]benzothiophene, a polycyclic aromatic compound, exhibits unique solubility characteristics that are of great interest in various fields, particularly in materials science and organic electronics. Here's what you should know about its solubility:

  • Non-polar nature: This compound tends to be non-polar due to its extensive fused ring structure, which often limits its solubility in polar solvents.
  • Solvent compatibility: Naphtho[2,3-f]benzothiophene is typically soluble in non-polar organic solvents such as benzene, toluene, and dichloromethane.
  • Temperature effects: Solubility can improve at elevated temperatures, making processes such as thermally-assisted dissolution a viable option for applications.
  • Potential for aggregation: Due to its planar structure, the compound may exhibit tendency toward aggregation in solution, affecting its solubility positively or negatively depending on the conditions.

In summary, while naphtho[2,3-f]benzothiophene demonstrates a clear preference for non-polar solvents, its solubility properties warrant careful consideration based on the application specifics, particularly in contexts where solvent selection is crucial.

Interesting facts

Interesting Facts about Naphtho[2,3-f]benzothiophene

Naphtho[2,3-f]benzothiophene is a fascinating organic compound that belongs to the class of polycyclic aromatic hydrocarbons. As a chemical scientist, it is intriguing to explore this compound due to its unique structure and potential applications. Here are some noteworthy aspects:

  • Structural Complexity: Naphtho[2,3-f]benzothiophene features a fusion of naphthalene and thiophene rings, showcasing remarkable structural diversity. This specific arrangement allows for interesting electronic properties.
  • Applications in Organic Electronics: Due to its semiconducting properties, naphtho[2,3-f]benzothiophene is considered for use in organic field-effect transistors (OFETs) and organic solar cells, contributing to advancements in flexible electronics.
  • Research and Development: Ongoing studies are investigating the compound's effectiveness in optoelectronic devices. Its ability to serve as an electron transport layer has implications for improving device efficiency.
  • Environmental Impact: Like many polycyclic aromatic hydrocarbons, it is crucial to understand the environmental behavior of naphtho[2,3-f]benzothiophene, especially regarding potential toxicity and biodegradation.
  • Chemical Reactivity: The presence of sulfur in thiophene adds an interesting aspect to its reactivity profile, and thus, it might serve as a valuable building block for synthesizing other complex organic molecules.

In conclusion, naphtho[2,3-f]benzothiophene represents an intersection of chemistry and technology. The compound not only enhances our understanding of molecular interactions but also opens doors to innovative applications in the ever-evolving field of materials science.

Synonyms
Anthra[2,3-b]thiophene
22108-55-0
ANTHRA(2,3-b)THIOPHENE
BRN 4416197
SCHEMBL4083703
SCHEMBL4083705
SCHEMBL4585002
DTXSID70176620