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1,5-bis(methylthio)naphthalene

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Identification
Molecular formula
C12H12S2
CAS number
22488-20-6
IUPAC name
1,5-bis(methylsulfanyl)naphthalene
State
State
Solid at room temperature characterized by a crystalline structure.
Melting point (Celsius)
57.00
Melting point (Kelvin)
330.00
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.00
General information
Molecular weight
202.32g/mol
Molar mass
202.3170g/mol
Density
1.2500g/cm3
Appearence

1,5-bis(methylsulfanyl)naphthalene is typically a pale yellow crystalline solid. It exhibits a lustrous sheen and is usually odorless though it may have a slight sulfide-like smell.

Comment on solubility

Solubility of 1,5-bis(methylsulfanyl)naphthalene (C12H12S2)

The solubility of 1,5-bis(methylsulfanyl)naphthalene, a compound characterized by its unique structure and functional groups, can be examined in several dimensions:

  • Solvent Polarity: This compound is expected to display a degree of solubility in organic solvents due to the presence of methyl sulfanyl (-Smethyl) groups, which can interact favorably with non-polar or weakly polar solvents.
  • Temperature Influence: Like many organic compounds, its solubility may increase with temperature, which enhances molecular interactions and helps overcome lattice energies.
  • Possible Limitations: However, solubility is often limited in polar solvents due to the non-polar naphthalene backbone, which generally tends to resist dissolving in high polar environments (e.g., water).

In summary, while 1,5-bis(methylsulfanyl)naphthalene may dissolve adequately in organic solvents such as hexane or chloroform, it may display low to negligible solubility in highly polar solvents. Thus, it is crucial to consider the solvent environment when evaluating the solubility of this compound.

Interesting facts

Interesting Facts about 1,5-bis(methylsulfanyl)naphthalene

1,5-bis(methylsulfanyl)naphthalene is a fascinating organic compound that belongs to the family of naphthalene derivatives, particularly notable for its dual methylsulfanyl groups positioned on the 1 and 5 carbon atoms. Here are some key insights into this unique compound:

  • Structure and Complexity: The structure of 1,5-bis(methylsulfanyl)naphthalene showcases an intriguing arrangement that contributes to its chemical properties. The presence of the methylsulfanyl groups enhances the compound's reactivity and may influence its photophysical characteristics.
  • Role in Organic Synthesis: This compound serves as a valuable building block in the field of organic chemistry. Compounds similar to 1,5-bis(methylsulfanyl)naphthalene are often utilized in the synthesis of various complex organic molecules, thereby playing a crucial role in drug discovery and materials science.
  • Environmental Considerations: Understanding the environmental impact of compounds containing sulfur groups is essential. 1,5-bis(methylsulfanyl)naphthalene and its derivatives may exhibit varying degrees of environmental persistence, making them subjects of interest in studies of pollution and remediation.
  • Biological Activity: Sulfur-containing compounds often demonstrate noteworthy biological activities. While specific studies may vary, methylthio substitutions can enhance the biological activity of naphthalene derivatives, potentially leading to applications in medicine.

In conclusion, 1,5-bis(methylsulfanyl)naphthalene exemplifies how subtle changes in molecular structure can yield compounds with versatile applications. Its role in organic synthesis, potential biological activities, and the study of its environmental impact make it a valuable subject within the realm of chemical research.

Synonyms
10075-74-8
Naphthalene, 1,5-bis(methylthio)-
DTXSID80143489
DTXCID5065980
1,5-Bis(methylsulfanyl)naphthalene
DYSPROSIUMCHLORIDE
1,5-dimethylthionaphthalene
TimTec1_005514
SCHEMBL14252184
1,5-di-(methylthio)-naphthalene
HMS1549K14
STK672222
AKOS005592751
NCGC00173146-01
ST4023323