CAS 291-21-4
:1,3,5-Trithiane
Description:
1,3,5-Trithiane is a cyclic thioether with the molecular formula C3H6S3. It features a six-membered ring structure containing three sulfur atoms and three carbon atoms, arranged alternately. This compound is typically a colorless liquid or solid at room temperature, characterized by a distinctive odor reminiscent of sulfur. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water. 1,3,5-Trithiane is known for its stability under normal conditions, although it can undergo oxidation or react with strong acids and bases. It is primarily used in organic synthesis and as a reagent in various chemical reactions, particularly in the preparation of sulfur-containing compounds. Additionally, it has applications in the field of materials science and as a potential precursor in the synthesis of pharmaceuticals. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C3H6S3
InChI:InChI=1S/C3H6S3/c1-4-2-6-3-5-1/h1-3H2
InChI key:InChIKey=LORRLQMLLQLPSJ-UHFFFAOYSA-N
SMILES:C1SCSCS1
Synonyms:- 1,3,5-Trithiacyclohexane
- 1,3,5-Trithiane
- 1,3,5-Trithiane (Sym.)
- Formaldehyde, thio-, trimer
- NSC 1937
- Thioform
- Thioformaldehyde trimer
- Trimethylene trisulfide
- Trithioformaldehyde
- s-Trithiane
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Found 4 products.
1,3,5-Trithiane
CAS:Formula:C3H6S3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:138.261,3,5-Trithiane
CAS:Controlled Product<p>Applications 1,3,5-Trithiane is an precursor to organosulfur reagents.<br>References Rakhimova, E.B., et al.: Russ. J. Org. Chem., 49, 1300 (2011); Reyes-L., et al.: J. Molec. Stru., 985, 134 (2011);<br></p>Formula:C3H6S3Color and Shape:NeatMolecular weight:138.27
