Interesting facts
Interesting Facts About 1,3,5-Trithiane
1,3,5-Trithiane is a fascinating compound that belongs to the class of thioethers, characterized by its unique arrangement of sulfur and carbon atoms. This compound has garnered attention in various fields of chemistry and materials science for several reasons:
- Structure: Its cyclic structure consists of three sulfur atoms and three carbon atoms, creating a six-membered ring. This specific arrangement influences its chemical reactivity and stability.
- Reactivity: 1,3,5-Trithiane is known for its ability to act as a sulfur source in various synthetic reactions. For instance, it can participate in nucleophilic substitution reactions, which are essential in organic synthesis.
- Versatility: This compound can be utilized in the preparation of other sulfur-containing compounds, making it an important building block in organic chemistry. Its derivatives have applications in the synthesis of pharmaceuticals and agrochemicals.
- Importance in Research: The study of 1,3,5-trithiane offers insights into the fundamental properties of sulfur-containing compounds. Researchers investigate its behavior and interactions under different conditions to better understand sulfides and their potential applications.
- Electronics and Materials Science: Sulfur-rich compounds like 1,3,5-trithiane are explored for their potential use in emerging technologies, including organic semiconductors and advanced materials because of their unique electronic properties.
As you've seen, 1,3,5-trithiane is more than just a simple compound. Its unique structure and versatile properties make it an intriguing subject of study and potential application in various scientific fields.
To quote a renowned chemist, “Understanding the sibling relationship between sulfur and carbon opens doors to remarkable innovations.” This highlights the compound’s significance in contributing to chemical discoveries and advancements.
Synonyms
1,3,5-TRITHIANE
291-21-4
s-Trithiane
sym-Trithian
Trithioformaldehyde
Thioform
Trimethylene trisulfide
1,3,5-Trithiacyclohexane
sym-Trithiane
Trimethylentrisulfid
Formaldehyde, thio-, trimer
Thioformaldehyde trimer
sym-Trithian [Czech]
1,3,5-trithian
NSC 1937
EINECS 206-029-7
BRN 0079834
4AM764YC6X
AI3-09774
NSC-1937
DTXSID2059778
CHEBI:39196
NSC1937
5-19-09-00105 (Beilstein Handbook Reference)
Thioform [Czech]
sym.-Trithiane
Trimethylentrisulfid [Czech]
Trithiometaformaldehyde
sTrithiane
symTrithian
1,5-Trithiane
1,3,5trithiane
MFCD00006653
S-Trithiane, 8CI
[1,3,5]trithiane
1,5-Trithiacyclohexane
Tris(methylene sulfide)
Formaldehyde, thio, trimer
WLN: T6S CS ESTJ
UNII-4AM764YC6X
SCHEMBL565045
1,3,5-Trithiane, 97%
DTXCID6037930
SCHEMBL16691831
1,3,5-TTCH
BBL100052
STL511026
AKOS005255575
AS-56659
DB-047528
NS00028636
T0532
D92358
Q2356063
206-029-7
Solubility of 1,3,5-trithiane
1,3,5-trithiane, with the chemical formula C3H6S3, is a fascinating sulfide compound that exhibits unique solubility characteristics. Its solubility can be influenced by several factors, including temperature, pressure, and the presence of other solvents.
Solubility Characteristics:
In summary, while 1,3,5-trithiane showcases significant solubility in organic environments, its interaction with polar solvents like water is quite minimal. This combination of properties makes it a versatile compound in the field of organic chemistry.