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Naphtho[2,3-g]benzothiophene

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Identification
Molecular formula
C16H10S
CAS number
272-64-8
IUPAC name
naphtho[2,3-g]benzothiophene
State
State

This compound is found as a solid at room temperature.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
525.00
Boiling point (Kelvin)
798.15
General information
Molecular weight
232.31g/mol
Molar mass
232.3100g/mol
Density
1.3000g/cm3
Appearence

Naphtho[2,3-g]benzothiophene is a pale yellow solid. It typically appears as yellow to orange crystals or powder.

Comment on solubility

Solubility of Naphtho[2,3-g]benzothiophene

Naphtho[2,3-g]benzothiophene, a polycyclic aromatic compound, exhibits intriguing solubility characteristics that are influenced by several factors:

  • Solvent Interaction: It is generally more soluble in organic solvents such as benzene, toluene, and dichloromethane. This is due to the non-polar nature of the compound, which interacts favorably with non-polar solvents.
  • Polarity Considerations: Being a hydrophobic compound, naphtho[2,3-g]benzothiophene exhibits very low to negligible solubility in water. This characteristic is important for its behavior in biological systems and environmental contexts.
  • Temperature Effects: As with many organic compounds, solubility can increase with temperature; thus, heating the solvent may enhance the dissolution of this compound.
  • Aggregation: In concentrated solutions, it may tend to aggregate, affecting its overall solubility properties and limiting its use in certain applications.

In summary, the solubility of naphtho[2,3-g]benzothiophene is predominantly dictated by its hydrophobic character, making it suitable for non-polar solvents, while exhibiting low interaction with water. Understanding its solubility can provide insights into its practical applications and behavior in various environments.

Interesting facts

Exploring Naphtho[2,3-g]benzothiophene

Naphtho[2,3-g]benzothiophene is a fascinating polycyclic aromatic hydrocarbon that captures the attention of chemists and material scientists alike. Here are some intriguing facts about this compound:

  • Structure and Uniqueness: This compound is characterized by a complex structure that features a fusion of naphthalene and benzothiophene rings. The unique arrangement contributes to its distinctive electronic and optical properties.
  • Applications in Materials Science: Due to its excellent electrical conductivity and stability, naphtho[2,3-g]benzothiophene is explored in the development of organic semiconductors and photovoltaic materials. Its potential for use in organic light-emitting diodes (OLEDs) is particularly promising.
  • Electronic Properties: Naphtho[2,3-g]benzothiophene exhibits interesting charge transport properties, making it a candidate for use in transistors. Researchers are studying its ability to facilitate charge mobility, which is crucial for efficient electronic devices.
  • Chemical Reactivity: The presence of the thiophene moiety in its structure enables unique chemical reactivity. The compound can participate in various chemical reactions, which are valuable for synthesizing new materials and compounds.
  • Health Considerations: Like many polycyclic aromatic hydrocarbons, naphtho[2,3-g]benzothiophene should be handled with caution. Research is ongoing to investigate its environmental impact and potential health effects on humans and wildlife.
  • Research and Development: The compound is still a subject of active research, with scientists exploring its potential applications in organic electronics, sensors, and even in pharmaceuticals.

As scientists continue to unlock the mysteries of naphtho[2,3-g]benzothiophene, it stands as a testament to the complexity and beauty of organic chemistry.

Synonyms
ANTHRA(1,2-b)THIOPHENE
anthra[1,2-b]thiophene
227-86-1
BRN 0156937
Anthro[1,2-b]thiophene
DTXSID20177228
Anthro(1,2-b)thiophene
DTXCID7099719