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2-(2-Methoxyphenyl)-1,3-dithiolane

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Identification
Molecular formula
C10H12OS2
CAS number
33859-64-4
IUPAC name
2-(2-methoxyphenyl)-1,3-dithiolane
State
State

Typically, at room temperature, 2-(2-Methoxyphenyl)-1,3-dithiolane is in a liquid state. Its viscosity is typical of organic liquids in this category.

Melting point (Celsius)
41.00
Melting point (Kelvin)
314.15
Boiling point (Celsius)
135.00
Boiling point (Kelvin)
408.15
General information
Molecular weight
200.30g/mol
Molar mass
200.3030g/mol
Density
1.1700g/cm3
Appearence

2-(2-Methoxyphenyl)-1,3-dithiolane appears as a colorless to pale yellow liquid. It has a distinctive odor and is typically clear and free from any particulate matter.

Comment on solubility

Solubility of 2-(2-methoxyphenyl)-1,3-dithiolane

2-(2-methoxyphenyl)-1,3-dithiolane exhibits unique solubility characteristics that can be influenced by various factors, including its molecular structure and the presence of functional groups. Here are some key points to consider regarding its solubility:

  • Polarity: The presence of the methoxy group increases the polarity of the compound, which may enhance its solubility in polar solvents.
  • Solvent Compatibility: It is likely to be soluble in organic solvents such as ethanol, methanol, or acetone, while showing limited solubility in water due to its hydrophobic dithiolane ring.
  • Temperature Dependency: Like many organic compounds, its solubility could increase with temperature, making it more soluble at elevated temperatures.
  • Structural Interactions: Intermolecular forces such as hydrogen bonding with the solvent can further influence the solubility of this compound.

Overall, 2-(2-methoxyphenyl)-1,3-dithiolane may be classified as having moderate solubility in polar organic solvents while being less soluble in aqueous solutions. This behavior emphasizes the importance of solvent choice in practical applications and experimental setups.

Interesting facts

Exploring 2-(2-methoxyphenyl)-1,3-dithiolane

2-(2-methoxyphenyl)-1,3-dithiolane is an intriguing compound that brings together both aromatic and heterocyclic chemistry. As a dithiolane, this compound features a five-membered ring containing two sulfur atoms, which contributes to its unique properties and reactivity. Here are some captivating facts about this compound:

  • Structural Diversity: The inclusion of the methoxy group on the phenyl ring enhances the compound's electronic properties, leading to a fascinating interplay of reactivity and stability.
  • Applications in Organic Synthesis: Compounds like 2-(2-methoxyphenyl)-1,3-dithiolane often serve as intermediates or building blocks in the synthesis of more complex molecules, particularly in the pharmaceutical and materials chemistry sectors.
  • Potential Biological Activity: Many dithiolanes exhibit interesting biological activities, including antioxidant properties, which makes them subjects of interest in medicinal chemistry.
  • Reactivity of Sulfur: The sulfur atoms in the dithiolane ring can participate in various chemical reactions, such as nucleophilic substitutions and redox processes, thus offering great synthetic utility.

As we delve deeper into the world of organic compounds, the study of such unique structures highlights not only their chemical significance but also their potential for innovative applications. The intricate balance between structural features and chemical behavior makes 2-(2-methoxyphenyl)-1,3-dithiolane a compelling focus for both research and development.

Synonyms
2-(2-Methoxyphenyl)-1,3-dithiolane
1,3-DITHIOLANE, 2-(o-METHOXYPHENYL)-
24588-76-9
DTXSID10179332
RefChem:1060892
DTXCID40101823
2-(o-Methoxyphenyl)-1,3-dithiolane
BRN 1244108
JKPYCJKJEBIDIG-UHFFFAOYSA-N
2-(2-Methoxyphenyl)-1,3-dithiolane #