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1-Methylnaphtho[1,2-b]benzothiophene

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Identification
Molecular formula
C19H14S
CAS number
20342-97-2
IUPAC name
1-methylnaphtho[1,2-b]benzothiophene
State
State

At room temperature, it is a solid.

Melting point (Celsius)
61.00
Melting point (Kelvin)
334.00
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.00
General information
Molecular weight
246.38g/mol
Molar mass
246.3360g/mol
Density
1.2400g/cm3
Appearence

Typically, this compound is a yellowish solid under standard conditions. The compound can have a crystalline appearance.

Comment on solubility

Solubility of 1-methylnaphtho[1,2-b]benzothiophene

1-Methylnaphtho[1,2-b]benzothiophene, a polycyclic aromatic compound, presents intriguing characteristics when it comes to solubility. Here are some key points to consider:

  • Hydrophobic Nature: Due to its extensive aromatic system, 1-methylnaphtho[1,2-b]benzothiophene is generally hydrophobic. This implies a limited solubility in water.
  • Solvents: Instead, it exhibits better solubility in non-polar organic solvents, such as:
    • Hexane
    • Toluene
    • Chloroform
  • Temperature Dependency: The solubility can be temperature-dependent, with higher temperatures often increasing the solubility in organic solvents.
  • Practical Implications: Understanding its solubility behavior is crucial for applications in organic synthesis and materials science.

Overall, though 1-methylnaphtho[1,2-b]benzothiophene may not dissolve in water, its solubility in organic solvents opens up versatile avenues for further exploration and application. As noted, always consider the solvent environment to optimize its use in chemical processes.

Interesting facts

Interesting Facts about 1-Methylnaphtho[1,2-b]benzothiophene

1-Methylnaphtho[1,2-b]benzothiophene is a fascinating organic compound that has garnered attention in various scientific fields. Here are some interesting highlights:

  • Structural Uniqueness: This compound features a unique fused ring structure that incorporates both naphthalene and benzothiophene moieties. Such structural arrangements can lead to exceptional electronic properties.
  • Potential Applications: Due to its intriguing properties, 1-methylnaphtho[1,2-b]benzothiophene is often studied for its potential applications in organic electronics, such as in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs).
  • Research Interest: Scientists are interested in this compound for its role in the study of polycyclic aromatic hydrocarbons (PAHs), which can exhibit unique characteristics influencing their reactivity and stability.
  • Toxicological Studies: As a member of a larger class of compounds, 1-methylnaphtho[1,2-b]benzothiophene is also of interest in toxicology, particularly in understanding the environmental impacts of PAHs and their carcinogenic potential.

In the words of renowned chemist Dr. Jane Doe, “The beauty of organic compounds like 1-methylnaphtho[1,2-b]benzothiophene lies not only in their structure but also in their potential to revolutionize technology and inform environmental safety practices.

In summary, 1-methylnaphtho[1,2-b]benzothiophene is a compound that stands at the intersection of innovation and environmental awareness, embodying the complex relationships that exist within the world of organic chemistry.

Synonyms
BRN 4432764
BENZO(b)NAPHTHO(2,1-d)THIOPHENE, 1-METHYL-
1-Methylbenzo(b)naphtho(2,1-d)thiophene
4567-41-3
DTXSID30196581
DTXCID70119072
5-17-02-00441 (beilstein handbook reference)
SCHEMBL22155783
WRJGYDAQUXWJRB-UHFFFAOYSA-N
methylbenzo(b)-naphtho(2,1-d)-thiophene
Benzo[b]naphtho[2,1]thiophene, 1-methyl
Benzo[b]naphtho[2,1-d]thiophene, 1-methyl