1,3-Dithiolane is a five-membered heterocyclic compound characterized by the presence of two sulfur atoms and three carbon atoms in its ring structure. The compound is known for its unique properties, including its ability to undergo various chemical reactions due to the presence of sulfur, which can participate in nucleophilic and electrophilic reactions. 1,3-Dithiolane is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents but has limited solubility in water. The compound is often used in organic synthesis, particularly in the formation of thioethers and as a protecting group for carbonyl compounds in synthetic chemistry. Additionally, 1,3-Dithiolane can exhibit interesting electrochemical properties, making it a subject of study in materials science and electrochemistry. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested. Overall, 1,3-Dithiolane is a versatile compound with applications in various fields of chemistry.

1,3-Dithiolane

4829-04-3: 1,3-Dithiacyclopentane, Dithiolane, NSC 193357, , 1,3-Dithiolane, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 

1,3-Dithiolane is an efficient method for the synthesis of 1,2-dithiane. The reaction is catalyzed by a strong acid and is asymmetric. This method has been shown to be effective in the synthesis of various ester compounds. 1,3-Dithiolane has also been used as an antibacterial agent. It inhibits bacterial growth by reducing free chloride ions in the cell membrane and blocking protein synthesis.

CAS 4829-04-3: 1,3-Dithiolane

1,3-Dithiolane

Ref: 3D-FD29253

1,3-DITHIOLANE

Ref: IN-DA003DL9

1,3-Dithiolane

Ref: 54-OR9080