Interesting facts
Interesting Facts about 4-methyl-2-phenyl-1,3-dithiolane
4-methyl-2-phenyl-1,3-dithiolane is a fascinating compound that belongs to the class of dithiolanes, known for their unique ring structure. This compound is particularly interesting due to several key features:
- Unique Structure: The presence of both sulfur atoms and a methyl and phenyl group in its structure gives it distinct chemical properties that make it a subject of study in organic chemistry.
- Reactivity: Dithiolanes can participate in various chemical reactions, including nucleophilic attacks and cycloadditions, making them versatile intermediates for synthesizing other compounds.
- Potential Applications: Compounds like 4-methyl-2-phenyl-1,3-dithiolane have potential applications in materials science, particularly in the development of new polymers and compounds that may exhibit specific electrical or optical properties.
- Natural Occurrence: Interestingly, some dithiolanes and their derivatives have been found in natural products, suggesting that they may play roles in biological systems.
In the world of organic synthesis, chemists often say: "Dithiolane derivatives pave the way for complex molecular architectures." This quote captures the essence of the compound's significance in synthetic chemistry. As research continues, it is likely that 4-methyl-2-phenyl-1,3-dithiolane will unveil even more intriguing aspects of its chemistry, further expanding our understanding of dithiolane structures and their interactions.
Synonyms
4-Methyl-2-phenyl-1,3-dithiolane
BRN 5508179
1,3-DITHIOLANE, 4-METHYL-2-PHENYL-
DTXSID10971535
DTXCID601399046
5616-53-5
SCHEMBL10956530
Solubility of 4-methyl-2-phenyl-1,3-dithiolane
The solubility of 4-methyl-2-phenyl-1,3-dithiolane can be described as intriguing and complex due to its unique molecular structure. This compound is primarily characterized as a heterocyclic compound that exhibits certain solubility behaviors:
In summary, the solubility of 4-methyl-2-phenyl-1,3-dithiolane can be characterized by its affinity for non-polar solvents while showing significant limitations in polar environments.